ENST00000236959.14:c.1281C>G
MANE Select
|
ENSP00000236959.9:p.Tyr427Ter
|
|
ENST00000236959.13:c.1281C>G
|
ENSP00000236959.9:p.Tyr427Ter
|
|
ENST00000426233.1:c.286C>G
|
|
|
ENST00000435675.5:c.1278C>G
|
ENSP00000415935.1:p.Tyr426Ter
|
|
ENST00000443953.5:c.*1378C>G
|
ENSP00000406792.1:n.*1378C>G
|
|
ENST00000446622.5:n.361C>G
|
|
|
ENST00000459796.1:n.92C>G
|
|
|
ENST00000467388.1:n.193C>G
|
|
|
ENST00000479093.5:n.196C>G
|
|
|
NM_004044.6:c.1281C>G
|
NP_004035.2:p.Tyr427Ter
|
|
XM_017004187.2:c.1281C>G
|
XP_016859676.1:p.Tyr427Ter
|
|
XM_024452919.1:c.1104C>G
|
XP_024308687.1:p.Tyr368Ter
|
|
NM_004044.7:c.1281C>G
MANE Select
|
NP_004035.2:p.Tyr427Ter
|
|