|
NM_015346.4:c.6144C>A
MANE Select
|
NP_056161.2:p.Tyr2048Ter
|
|
ENST00000347230.9:c.6144C>A
MANE Select
|
ENSP00000251119.5:p.Tyr2048Ter
|
|
NM_015346.3:c.6144C>A
|
NP_056161.2:p.Tyr2048Ter
|
|
ENST00000347230.8:c.6144C>A
|
ENSP00000251119.5:p.Tyr2048Ter
|
|
ENST00000394455.6:n.1407C>A
|
|
|
ENST00000554523.5:n.6281C>A
|
|
|
ENST00000554557.5:c.*4122C>A
|
ENSP00000450431.1:n.*4122C>A
|
|
ENST00000555452.1:c.6144C>A
|
ENSP00000450603.1:p.Tyr2048Ter
|
|
ENST00000676512.1:c.6162C>A
|
ENSP00000504552.1:p.Tyr2054Ter
|
|
ENST00000676620.1:c.6066C>A
|
ENSP00000504587.1:p.Tyr2022Ter
|
|
ENST00000678386.1:c.6189C>A
|
ENSP00000503677.1:p.Tyr2063Ter
|
|
XM_006720093.2:c.6144C>A
|
XP_006720156.1:p.Tyr2048Ter
|
|
XM_011536606.1:c.4635C>A
|
XP_011534908.1:p.Tyr1545Ter
|
|
XM_011536607.1:c.3819C>A
|
XP_011534909.1:p.Tyr1273Ter
|
|
XM_011536608.1:c.3726C>A
|
XP_011534910.1:p.Tyr1242Ter
|
|
XM_017021124.1:c.6162C>A
|
XP_016876613.1:p.Tyr2054Ter
|
|
XM_017021125.1:c.6162C>A
|
XP_016876614.1:p.Tyr2054Ter
|
|
XM_017021126.1:c.4653C>A
|
XP_016876615.1:p.Tyr1551Ter
|
|
XM_017021127.2:c.3837C>A
|
XP_016876616.1:p.Tyr1279Ter
|
|
XM_017021128.1:c.3744C>A
|
XP_016876617.1:p.Tyr1248Ter
|