ENST00000472420.6:n.376C=
|
|
|
ENST00000681993.1:n.849C=
|
|
|
ENST00000682295.1:c.452C=
|
ENSP00000507499.1:n.452C=
|
|
ENST00000682303.1:c.*3083C=
|
ENSP00000508325.1:n.*3083C=
|
|
ENST00000682308.1:c.3297C=
|
ENSP00000507056.1:p.Gly1099=
|
|
ENST00000682480.1:c.3315C=
|
ENSP00000508344.1:p.Gly1105=
|
|
ENST00000682546.1:c.3294C=
|
ENSP00000508188.1:p.Gly1098=
|
|
ENST00000682585.1:c.3297C=
|
ENSP00000506885.1:p.Gly1099=
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|
ENST00000682595.1:n.3881C=
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|
|
ENST00000682607.1:c.1715C=
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|
|
ENST00000682612.1:c.149C=
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|
|
ENST00000682779.1:c.3288C=
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ENSP00000507947.1:p.Gly1096=
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|
ENST00000682845.1:n.2399C=
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|
|
ENST00000682885.1:c.3252C=
|
ENSP00000508036.1:p.Gly1084=
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|
ENST00000682933.1:n.3371C=
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|
|
ENST00000683002.1:c.149C=
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|
|
ENST00000683072.1:n.3881C=
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|
|
ENST00000683080.1:n.916C=
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|
|
ENST00000683125.1:c.3405C=
|
ENSP00000507939.1:p.Gly1135=
|
|
ENST00000683213.1:c.3300C=
|
ENSP00000507751.1:p.Gly1100=
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|
ENST00000683220.1:c.3327C=
|
ENSP00000507151.1:p.Gly1109=
|
|
ENST00000683329.1:n.4100C=
|
|
|
ENST00000683346.1:c.*3172C=
|
ENSP00000507458.1:n.*3172C=
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|
ENST00000683409.1:n.1904C=
|
|
|
ENST00000683459.1:n.3884C=
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|
|
ENST00000683528.1:c.149C=
|
|
|
ENST00000683590.1:c.3045C=
|
ENSP00000506820.1:p.Gly1015=
|
|
ENST00000683623.1:c.3204C=
|
ENSP00000507702.1:p.Gly1068=
|
|
ENST00000683645.1:n.3848C=
|
|
|
ENST00000683796.1:c.*3169C=
|
ENSP00000508221.1:n.*3169C=
|
|
ENST00000683802.1:n.6222C=
|
|
|
ENST00000683833.1:c.3288C=
|
ENSP00000506852.1:p.Gly1096=
|
|
ENST00000683994.1:c.3297C=
|
ENSP00000507181.1:p.Gly1099=
|
|
ENST00000684290.1:c.*833C=
|
ENSP00000507243.1:n.*833C=
|
|
ENST00000684306.1:c.*3210C=
|
ENSP00000508384.1:n.*3210C=
|
|
ENST00000684341.1:n.3317C=
|
|
|
ENST00000684383.1:c.*2935C=
|
ENSP00000506863.1:n.*2935C=
|
|
ENST00000684418.1:n.4478C=
|
|
|
ENST00000684454.1:n.2647C=
|
|
|
ENST00000684619.1:c.*3169C=
|
ENSP00000508088.1:n.*3169C=
|
|
ENST00000684743.1:n.4328C=
|
|
|
ENST00000260665.12:c.3297C=
MANE Select
|
ENSP00000260665.7:p.Gly1099=
|
|
ENST00000260665.11:c.3297C=
|
ENSP00000260665.7:p.Gly1099=
|
|
NM_133259.3:c.3297C=
|
NP_573566.2:p.Gly1099=
|
|
XM_006711915.2:c.3219C=
|
XP_006711978.1:p.Gly1073=
|
|
XM_011532473.1:c.3297C=
|
XP_011530775.1:p.Gly1099=
|
|
XM_011532474.1:c.3297C=
|
XP_011530776.1:p.Gly1099=
|
|
XM_017003117.1:c.3219C=
|
XP_016858606.1:p.Gly1073=
|
|
XR_002958896.1:n.3339C=
|
|
|
NM_133259.4:c.3297C=
MANE Select
|
NP_573566.2:p.Gly1099=
|
|