ENST00000696170.1:c.*100C>T
|
ENSP00000512461.1:n.*100C>T
|
|
ENST00000696171.1:c.495C>T
|
ENSP00000512462.1:p.Ile165=
|
|
ENST00000696172.1:c.338-2897C>T
|
ENSP00000512463.1:n.338-2897C>T
|
|
ENST00000378588.5:c.591C>T
MANE Select
|
ENSP00000367851.4:p.Ile197=
|
|
ENST00000378588.4:c.591C>T
|
ENSP00000367851.4:p.Ile197=
|
|
ENST00000465127.1:c.171+370058C>T
|
ENSP00000417050.1:n.171+370058C>T
|
|
NM_000397.3:c.591C>T , LRG_53t1:c.591C>T
|
NP_000388.2:p.Ile197=
|
|
XM_011543890.1:c.285C>T
|
XP_011542192.1:p.Ile95=
|
|
NM_000397.4:c.591C>T
MANE Select
|
NP_000388.2:p.Ile197=
|
|