ENST00000696170.1:c.168T>C
|
ENSP00000512461.1:p.Pro56=
|
|
ENST00000696171.1:c.72T>C
|
ENSP00000512462.1:p.Pro24=
|
|
ENST00000696172.1:c.168T>C
|
ENSP00000512463.1:p.Pro56=
|
|
ENST00000696173.1:n.176T>C
|
|
|
ENST00000378588.5:c.168T>C
MANE Select
|
ENSP00000367851.4:p.Pro56=
|
|
ENST00000378588.4:c.168T>C
|
ENSP00000367851.4:p.Pro56=
|
|
ENST00000465127.1:c.171+357516T>C
|
ENSP00000417050.1:n.171+357516T>C
|
|
NM_000397.3:c.168T>C , LRG_53t1:c.168T>C
|
NP_000388.2:p.Pro56=
|
|
XM_011543890.1:c.-263T>C
|
XP_011542192.1:n.-263T>C
|
|
NM_000397.4:c.168T>C
MANE Select
|
NP_000388.2:p.Pro56=
|
|