ENST00000696170.1:c.*109T>A
|
ENSP00000512461.1:n.*109T>A
|
|
ENST00000696171.1:c.504T>A
|
ENSP00000512462.1:p.Ser168=
|
|
ENST00000696172.1:c.338-2888T>A
|
ENSP00000512463.1:n.338-2888T>A
|
|
ENST00000378588.5:c.600T>A
MANE Select
|
ENSP00000367851.4:p.Ser200=
|
|
ENST00000378588.4:c.600T>A
|
ENSP00000367851.4:p.Ser200=
|
|
ENST00000465127.1:c.171+370067T>A
|
ENSP00000417050.1:n.171+370067T>A
|
|
NM_000397.3:c.600T>A , LRG_53t1:c.600T>A
|
NP_000388.2:p.Ser200=
|
|
XM_011543890.1:c.294T>A
|
XP_011542192.1:p.Ser98=
|
|
NM_000397.4:c.600T>A
MANE Select
|
NP_000388.2:p.Ser200=
|
|