ENST00000355265.7:c.565A>T
MANE Select
|
ENSP00000347409.2:p.Asn189Tyr
|
|
ENST00000467543.6:c.*417A>T
|
ENSP00000420011.2:n.*417A>T
|
|
ENST00000355265.6:c.565A>T
|
ENSP00000347409.2:p.Asn189Tyr
|
|
ENST00000467543.5:c.508A>T
|
ENSP00000420011.1:p.Asn170Tyr
|
|
ENST00000476829.5:c.525+370A>T
|
ENSP00000419889.1:n.525+370A>T
|
|
ENST00000479768.6:n.683A>T
|
|
|
ENST00000494148.1:n.164A>T
|
|
|
NM_000420.2:c.565A>T
|
NP_000411.1:p.Asn189Tyr
|
|
XM_005249993.2:c.601A>T
|
XP_005250050.1:p.Asn201Tyr
|
|
NM_000420.3:c.565A>T
MANE Select
|
NP_000411.1:p.Asn189Tyr
|
|