ENST00000673918.2:c.4874C>A
|
ENSP00000501283.1:p.Pro1625His
|
|
ENST00000674114.2:c.2481C>A
|
ENSP00000501039.2:n.2481C>A
|
|
ENST00000684977.1:c.158C>A
|
ENSP00000509384.1:p.Pro53His
|
|
ENST00000685168.1:c.366C>A
|
|
|
ENST00000689544.1:n.93C>A
|
|
|
ENST00000691421.1:c.161C>A
|
ENSP00000508674.1:p.Pro54His
|
|
ENST00000691855.1:c.4482C>A
|
|
|
ENST00000692961.1:c.4940C>A
|
ENSP00000509289.1:p.Pro1647His
|
|
ENST00000420124.4:c.4940C>A
MANE Select
|
ENSP00000398837.2:p.Pro1647His
|
|
ENST00000673918.1:c.4874C>A
|
ENSP00000501283.1:p.Pro1625His
|
|
ENST00000674114.1:c.2262C>A
|
|
|
ENST00000420124.2:c.4940C>A
|
ENSP00000398837.1:p.Pro1647His
|
|
NM_014727.2:c.4940C>A
|
NP_055542.1:p.Pro1647His
|
|
XM_011527561.1:c.4874C>A
|
XP_011525863.1:p.Pro1625His
|
|
XM_011527562.1:c.4940C>A
|
XP_011525864.1:p.Pro1647His
|
|
XM_011527563.1:c.4664C>A
|
XP_011525865.1:p.Pro1555His
|
|
XM_011527561.2:c.4376C>A
|
XP_011525863.2:p.Pro1459His
|
|
XM_011527562.2:c.4940C>A
|
XP_011525864.1:p.Pro1647His
|
|
XM_017027544.1:c.4940C>A
|
XP_016883033.1:p.Pro1647His
|
|
XM_017027545.1:c.4376C>A
|
XP_016883034.1:p.Pro1459His
|
|
XM_017027546.1:c.1904C>A
|
XP_016883035.1:p.Pro635His
|
|
NM_014727.3:c.4940C>A
MANE Select
|
NP_055542.1:p.Pro1647His
|
|