ENST00000682275.1:c.1882G>A
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ENSP00000507852.1:p.Ala628Thr
|
|
ENST00000683395.1:c.1823G>A
|
|
|
ENST00000684087.1:c.1846G>A
|
ENSP00000506978.1:p.Ala616Thr
|
|
ENST00000506362.2:c.1597G>A
|
ENSP00000424103.2:p.Ala533Thr
|
|
ENST00000673642.1:c.1505G>A
|
ENSP00000501242.1:n.1505G>A
|
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ENST00000673991.1:c.1882G>A
|
ENSP00000501033.1:p.Ala628Thr
|
|
ENST00000226760.5:c.1846G>A
MANE Select
|
ENSP00000226760.1:p.Ala616Thr
|
|
ENST00000503569.5:c.1846G>A
|
ENSP00000423337.1:p.Ala616Thr
|
|
ENST00000507765.1:n.2031G>A
|
|
|
NM_001145853.1:c.1846G>A
|
NP_001139325.1:p.Ala616Thr
|
|
NM_006005.3:c.1846G>A
MANE Select
|
NP_005996.2:p.Ala616Thr
|
|
XM_017008586.1:c.1855G>A
|
XP_016864075.1:p.Ala619Thr
|
|