ENST00000696170.1:c.*149A=
|
ENSP00000512461.1:n.*149A=
|
|
ENST00000696171.1:c.544A=
|
ENSP00000512462.1:p.Ile182=
|
|
ENST00000696172.1:c.338-2848A=
|
ENSP00000512463.1:n.338-2848A=
|
|
ENST00000378588.5:c.640A=
MANE Select
|
ENSP00000367851.4:p.Ile214=
|
|
ENST00000378588.4:c.640A=
|
ENSP00000367851.4:p.Ile214=
|
|
ENST00000465127.1:c.171+370107A=
|
ENSP00000417050.1:n.171+370107A=
|
|
NM_000397.3:c.640A= , LRG_53t1:c.640A=
|
NP_000388.2:p.Ile214=
|
|
XM_011543890.1:c.334A=
|
XP_011542192.1:p.Ile112=
|
|
NM_000397.4:c.640A=
MANE Select
|
NP_000388.2:p.Ile214=
|
|