ENST00000696170.1:c.*19T>C
|
ENSP00000512461.1:n.*19T>C
|
|
ENST00000696171.1:c.414T>C
|
ENSP00000512462.1:p.Ala138=
|
|
ENST00000696172.1:c.338-2978T>C
|
ENSP00000512463.1:n.338-2978T>C
|
|
ENST00000378588.5:c.510T>C
MANE Select
|
ENSP00000367851.4:p.Ala170=
|
|
ENST00000378588.4:c.510T>C
|
ENSP00000367851.4:p.Ala170=
|
|
ENST00000465127.1:c.171+369977T>C
|
ENSP00000417050.1:n.171+369977T>C
|
|
NM_000397.3:c.510T>C , LRG_53t1:c.510T>C
|
NP_000388.2:p.Ala170=
|
|
XM_011543890.1:c.204T>C
|
XP_011542192.1:p.Ala68=
|
|
NM_000397.4:c.510T>C
MANE Select
|
NP_000388.2:p.Ala170=
|
|