|
ENST00000472420.6:n.357C=
|
|
|
|
ENST00000681993.1:n.830C=
|
|
|
|
ENST00000682295.1:c.433C=
|
ENSP00000507499.1:n.433C=
|
|
|
ENST00000682303.1:c.*3064C=
|
ENSP00000508325.1:n.*3064C=
|
|
|
ENST00000682308.1:c.3278C=
|
ENSP00000507056.1:p.Ala1093=
|
|
|
ENST00000682480.1:c.3296C=
|
ENSP00000508344.1:p.Ala1099=
|
|
|
ENST00000682546.1:c.3275C=
|
ENSP00000508188.1:p.Ala1092=
|
|
|
ENST00000682585.1:c.3278C=
|
ENSP00000506885.1:p.Ala1093=
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|
|
ENST00000682595.1:n.3862C=
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|
|
|
ENST00000682607.1:c.1696C=
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|
|
|
ENST00000682612.1:c.130C=
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|
|
|
ENST00000682779.1:c.3269C=
|
ENSP00000507947.1:p.Ala1090=
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|
|
ENST00000682845.1:n.2380C=
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|
|
|
ENST00000682885.1:c.3233C=
|
ENSP00000508036.1:p.Ala1078=
|
|
|
ENST00000682933.1:n.3352C=
|
|
|
|
ENST00000683002.1:c.130C=
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|
|
|
ENST00000683072.1:n.3862C=
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|
|
|
ENST00000683080.1:n.897C=
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|
|
|
ENST00000683125.1:c.3386C=
|
ENSP00000507939.1:p.Ala1129=
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|
|
ENST00000683213.1:c.3281C=
|
ENSP00000507751.1:p.Ala1094=
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|
|
ENST00000683220.1:c.3308C=
|
ENSP00000507151.1:p.Ala1103=
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|
|
ENST00000683329.1:n.4081C=
|
|
|
|
ENST00000683346.1:c.*3153C=
|
ENSP00000507458.1:n.*3153C=
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|
|
ENST00000683409.1:n.1885C=
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|
|
|
ENST00000683459.1:n.3865C=
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|
ENST00000683528.1:c.130C=
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|
|
ENST00000683590.1:c.3026C=
|
ENSP00000506820.1:p.Ala1009=
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|
|
ENST00000683623.1:c.3185C=
|
ENSP00000507702.1:p.Ala1062=
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|
|
ENST00000683645.1:n.3829C=
|
|
|
|
ENST00000683796.1:c.*3150C=
|
ENSP00000508221.1:n.*3150C=
|
|
|
ENST00000683802.1:n.6203C=
|
|
|
|
ENST00000683833.1:c.3269C=
|
ENSP00000506852.1:p.Ala1090=
|
|
|
ENST00000683994.1:c.3278C=
|
ENSP00000507181.1:p.Ala1093=
|
|
|
ENST00000684290.1:c.*814C=
|
ENSP00000507243.1:n.*814C=
|
|
|
ENST00000684306.1:c.*3191C=
|
ENSP00000508384.1:n.*3191C=
|
|
|
ENST00000684341.1:n.3298C=
|
|
|
|
ENST00000684383.1:c.*2916C=
|
ENSP00000506863.1:n.*2916C=
|
|
|
ENST00000684418.1:n.4459C=
|
|
|
|
ENST00000684454.1:n.2628C=
|
|
|
|
ENST00000684619.1:c.*3150C=
|
ENSP00000508088.1:n.*3150C=
|
|
|
ENST00000684743.1:n.4309C=
|
|
|
|
ENST00000260665.12:c.3278C=
MANE Select
|
ENSP00000260665.7:p.Ala1093=
|
|
|
ENST00000260665.11:c.3278C=
|
ENSP00000260665.7:p.Ala1093=
|
|
|
NM_133259.3:c.3278C=
|
NP_573566.2:p.Ala1093=
|
|
|
XM_006711915.2:c.3200C=
|
XP_006711978.1:p.Ala1067=
|
|
|
XM_011532473.1:c.3278C=
|
XP_011530775.1:p.Ala1093=
|
|
|
XM_011532474.1:c.3278C=
|
XP_011530776.1:p.Ala1093=
|
|
|
XM_017003117.1:c.3200C=
|
XP_016858606.1:p.Ala1067=
|
|
|
XR_002958896.1:n.3320C=
|
|
|
|
NM_133259.4:c.3278C=
MANE Select
|
NP_573566.2:p.Ala1093=
|
|
