ENST00000696170.1:c.142T=
|
ENSP00000512461.1:p.Ser48=
|
|
ENST00000696171.1:c.46T=
|
ENSP00000512462.1:p.Ser16=
|
|
ENST00000696172.1:c.142T=
|
ENSP00000512463.1:p.Ser48=
|
|
ENST00000696173.1:n.150T=
|
|
|
ENST00000378588.5:c.142T=
MANE Select
|
ENSP00000367851.4:p.Ser48=
|
|
ENST00000378588.4:c.142T=
|
ENSP00000367851.4:p.Ser48=
|
|
ENST00000465127.1:c.171+357490T=
|
ENSP00000417050.1:n.171+357490T=
|
|
NM_000397.3:c.142T= , LRG_53t1:c.142T=
|
NP_000388.2:p.Ser48=
|
|
XM_011543890.1:c.-289T=
|
XP_011542192.1:n.-289T=
|
|
NM_000397.4:c.142T=
MANE Select
|
NP_000388.2:p.Ser48=
|
|