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ENST00000419884.6:c.555G=
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ENST00000681993.1:n.1477G=
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ENST00000682154.1:n.1359G=
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ENST00000682303.1:c.*3636G=
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ENSP00000508325.1:n.*3636G=
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ENST00000682308.1:c.3850G=
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ENSP00000507056.1:p.Glu1284=
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ENST00000682434.1:n.3480G=
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ENST00000682480.1:c.3943G=
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ENSP00000508344.1:p.Glu1315=
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ENST00000682546.1:c.3922G=
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ENSP00000508188.1:p.Glu1308=
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ENST00000682585.1:c.*53G=
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ENSP00000506885.1:n.*53G=
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ENST00000682607.1:c.2668G=
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ENST00000682612.1:c.752+2029G=
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ENST00000682696.1:c.25G=
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ENSP00000508411.1:p.Glu9=
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ENST00000682779.1:c.3916G=
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ENSP00000507947.1:p.Glu1306=
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ENST00000682885.1:c.3880G=
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ENSP00000508036.1:p.Glu1294=
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ENST00000682933.1:n.4125G=
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ENST00000683002.1:c.777G=
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ENST00000683072.1:n.4509G=
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ENST00000683080.1:n.1544G=
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ENST00000683096.1:n.2366G=
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ENST00000683125.1:c.4033G=
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ENSP00000507939.1:p.Glu1345=
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ENST00000683213.1:c.3928G=
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ENSP00000507751.1:p.Glu1310=
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ENST00000683220.1:c.3955G=
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ENSP00000507151.1:p.Glu1319=
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ENST00000683329.1:n.4728G=
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ENST00000683346.1:c.*3800G=
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ENSP00000507458.1:n.*3800G=
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ENST00000683409.1:n.2457G=
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ENST00000683459.1:n.4512G=
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ENST00000683590.1:c.3598G=
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ENSP00000506820.1:p.Glu1200=
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ENST00000683623.1:c.3832G=
|
ENSP00000507702.1:p.Glu1278=
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ENST00000683796.1:c.*3722G=
|
ENSP00000508221.1:n.*3722G=
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ENST00000683833.1:c.3841G=
|
ENSP00000506852.1:p.Glu1281=
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|
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ENST00000683994.1:c.*38G=
|
ENSP00000507181.1:n.*38G=
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ENST00000684290.1:c.*1386G=
|
ENSP00000507243.1:n.*1386G=
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ENST00000684306.1:c.*3838G=
|
ENSP00000508384.1:n.*3838G=
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ENST00000684383.1:c.*3563G=
|
ENSP00000506863.1:n.*3563G=
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ENST00000684418.1:n.5106G=
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ENST00000684433.1:n.309G=
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ENST00000684454.1:n.7789G=
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ENST00000684619.1:c.*3797G=
|
ENSP00000508088.1:n.*3797G=
|
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ENST00000684743.1:n.6670G=
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|
ENST00000260665.12:c.3925G=
MANE Select
|
ENSP00000260665.7:p.Glu1309=
|
|
|
ENST00000260665.11:c.3925G=
|
ENSP00000260665.7:p.Glu1309=
|
|
|
ENST00000419884.5:c.166G=
|
ENSP00000414207.1:p.Glu56=
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|
ENST00000463456.5:n.2968G=
|
|
|
|
NM_133259.3:c.3925G=
|
NP_573566.2:p.Glu1309=
|
|
|
XM_006711915.2:c.3847G=
|
XP_006711978.1:p.Glu1283=
|
|
|
XM_011532473.1:c.3850G=
|
XP_011530775.1:p.Glu1284=
|
|
|
XM_011532474.1:c.3925G=
|
XP_011530776.1:p.Glu1309=
|
|
|
XM_017003117.1:c.3772G=
|
XP_016858606.1:p.Glu1258=
|
|
|
XR_002958896.1:n.3967G=
|
|
|
|
NM_133259.4:c.3925G=
MANE Select
|
NP_573566.2:p.Glu1309=
|
|
