ENST00000703783.1:n.937C>G
|
|
|
ENST00000703785.1:n.1018C>G
|
|
|
ENST00000262464.9:c.4153C>G
MANE Select
|
ENSP00000262464.4:p.Leu1385Val
|
|
ENST00000262464.8:c.4153C>G
|
ENSP00000262464.4:p.Leu1385Val
|
|
ENST00000507835.5:c.703C>G
|
ENSP00000426839.1:p.Leu235Val
|
|
ENST00000508053.5:c.4153C>G
|
ENSP00000424571.1:p.Leu1385Val
|
|
ENST00000508989.5:c.4054C>G
|
ENSP00000425596.1:p.Leu1352Val
|
|
ENST00000619499.4:c.4150C>G
|
ENSP00000482132.1:p.Leu1384Val
|
|
NM_001999.3:c.4153C>G
|
NP_001990.2:p.Leu1385Val
|
|
XM_017009228.2:c.4000C>G
|
XP_016864717.1:p.Leu1334Val
|
|
NM_001999.4:c.4153C>G
MANE Select
|
NP_001990.2:p.Leu1385Val
|
|