ENST00000696170.1:c.343T>G
|
ENSP00000512461.1:p.Ter115Gly
|
|
ENST00000696171.1:c.393T>G
|
ENSP00000512462.1:p.Pro131=
|
|
ENST00000696172.1:c.338-2999T>G
|
ENSP00000512463.1:n.338-2999T>G
|
|
ENST00000378588.5:c.489T>G
MANE Select
|
ENSP00000367851.4:p.Pro163=
|
|
ENST00000378588.4:c.489T>G
|
ENSP00000367851.4:p.Pro163=
|
|
ENST00000465127.1:c.171+369956T>G
|
ENSP00000417050.1:n.171+369956T>G
|
|
NM_000397.3:c.489T>G , LRG_53t1:c.489T>G
|
NP_000388.2:p.Pro163=
|
|
XM_011543890.1:c.183T>G
|
XP_011542192.1:p.Pro61=
|
|
NM_000397.4:c.489T>G
MANE Select
|
NP_000388.2:p.Pro163=
|
|