ENST00000673918.2:c.4924T>G
|
ENSP00000501283.1:p.Phe1642Val
|
|
ENST00000674114.2:c.2531T>G
|
ENSP00000501039.2:n.2531T>G
|
|
ENST00000684977.1:c.208T>G
|
ENSP00000509384.1:p.Phe70Val
|
|
ENST00000685168.1:c.416T>G
|
|
|
ENST00000689544.1:n.143T>G
|
|
|
ENST00000691421.1:c.211T>G
|
ENSP00000508674.1:p.Phe71Val
|
|
ENST00000691855.1:c.4532T>G
|
|
|
ENST00000692961.1:c.4990T>G
|
ENSP00000509289.1:p.Phe1664Val
|
|
ENST00000420124.4:c.4990T>G
MANE Select
|
ENSP00000398837.2:p.Phe1664Val
|
|
ENST00000673918.1:c.4924T>G
|
ENSP00000501283.1:p.Phe1642Val
|
|
ENST00000674114.1:c.2312T>G
|
|
|
ENST00000420124.2:c.4990T>G
|
ENSP00000398837.1:p.Phe1664Val
|
|
NM_014727.2:c.4990T>G
|
NP_055542.1:p.Phe1664Val
|
|
XM_011527561.1:c.4924T>G
|
XP_011525863.1:p.Phe1642Val
|
|
XM_011527562.1:c.4990T>G
|
XP_011525864.1:p.Phe1664Val
|
|
XM_011527563.1:c.4714T>G
|
XP_011525865.1:p.Phe1572Val
|
|
XM_011527561.2:c.4426T>G
|
XP_011525863.2:p.Phe1476Val
|
|
XM_011527562.2:c.4990T>G
|
XP_011525864.1:p.Phe1664Val
|
|
XM_017027544.1:c.4990T>G
|
XP_016883033.1:p.Phe1664Val
|
|
XM_017027545.1:c.4426T>G
|
XP_016883034.1:p.Phe1476Val
|
|
XM_017027546.1:c.1954T>G
|
XP_016883035.1:p.Phe652Val
|
|
NM_014727.3:c.4990T>G
MANE Select
|
NP_055542.1:p.Phe1664Val
|
|