ENST00000673918.2:c.4883C=
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ENSP00000501283.1:p.Thr1628=
|
|
ENST00000674114.2:c.2490C=
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ENSP00000501039.2:n.2490C=
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ENST00000684977.1:c.167C=
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ENSP00000509384.1:p.Thr56=
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ENST00000685168.1:c.375C=
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ENST00000689544.1:n.102C=
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ENST00000691421.1:c.170C=
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ENSP00000508674.1:p.Thr57=
|
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ENST00000691855.1:c.4491C=
|
|
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ENST00000692961.1:c.4949C=
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ENSP00000509289.1:p.Thr1650=
|
|
ENST00000420124.4:c.4949C=
MANE Select
|
ENSP00000398837.2:p.Thr1650=
|
|
ENST00000673918.1:c.4883C=
|
ENSP00000501283.1:p.Thr1628=
|
|
ENST00000674114.1:c.2271C=
|
|
|
ENST00000420124.2:c.4949C=
|
ENSP00000398837.1:p.Thr1650=
|
|
NM_014727.2:c.4949C=
|
NP_055542.1:p.Thr1650=
|
|
XM_011527561.1:c.4883C=
|
XP_011525863.1:p.Thr1628=
|
|
XM_011527562.1:c.4949C=
|
XP_011525864.1:p.Thr1650=
|
|
XM_011527563.1:c.4673C=
|
XP_011525865.1:p.Thr1558=
|
|
XM_011527561.2:c.4385C=
|
XP_011525863.2:p.Thr1462=
|
|
XM_011527562.2:c.4949C=
|
XP_011525864.1:p.Thr1650=
|
|
XM_017027544.1:c.4949C=
|
XP_016883033.1:p.Thr1650=
|
|
XM_017027545.1:c.4385C=
|
XP_016883034.1:p.Thr1462=
|
|
XM_017027546.1:c.1913C=
|
XP_016883035.1:p.Thr638=
|
|
NM_014727.3:c.4949C=
MANE Select
|
NP_055542.1:p.Thr1650=
|
|