ENST00000355265.7:c.649T>A
MANE Select
|
ENSP00000347409.2:p.Ser217Thr
|
|
ENST00000467543.6:c.*501T>A
|
ENSP00000420011.2:n.*501T>A
|
|
ENST00000355265.6:c.649T>A
|
ENSP00000347409.2:p.Ser217Thr
|
|
ENST00000467543.5:c.592T>A
|
ENSP00000420011.1:p.Ser198Thr
|
|
ENST00000476829.5:c.525+454T>A
|
ENSP00000419889.1:n.525+454T>A
|
|
ENST00000479768.6:n.767T>A
|
|
|
ENST00000494148.1:n.248T>A
|
|
|
NM_000420.2:c.649T>A
|
NP_000411.1:p.Ser217Thr
|
|
XM_005249993.2:c.685T>A
|
XP_005250050.1:p.Ser229Thr
|
|
NM_000420.3:c.649T>A
MANE Select
|
NP_000411.1:p.Ser217Thr
|
|