ENST00000428701.6:n.560G>C
|
|
|
ENST00000360323.11:c.456G>C
MANE Select
|
ENSP00000353472.6:p.Glu152Asp
|
|
ENST00000360323.10:c.456G>C
|
ENSP00000353472.6:p.Glu152Asp
|
|
ENST00000376815.3:c.343+339G>C
|
ENSP00000366011.3:n.343+339G>C
|
|
ENST00000376818.7:c.343+339G>C
|
ENSP00000366014.3:n.343+339G>C
|
|
ENST00000376828.6:c.471G>C
|
ENSP00000366024.2:p.Glu157Asp
|
|
ENST00000428701.5:c.456G>C
|
ENSP00000412927.1:p.Glu152Asp
|
|
ENST00000478355.5:n.456G>C
|
|
|
ENST00000478519.5:c.343+339G>C
|
ENSP00000436375.1:n.343+339G>C
|
|
NM_002127.5:c.456G>C
|
NP_002118.1:p.Glu152Asp
|
|
NM_001363567.1:c.471G>C
|
NP_001350496.1:p.Glu157Asp
|
|
XM_017010817.1:c.343+339G>C
|
XP_016866306.1:n.343+339G>C
|
|
XM_017010818.1:c.343+339G>C
|
XP_016866307.1:n.343+339G>C
|
|
XM_024446420.1:c.456G>C
|
XP_024302188.1:p.Glu152Asp
|
|
NM_001363567.2:c.471G>C
|
NP_001350496.1:p.Glu157Asp
|
|
NM_001384280.1:c.471G>C
|
NP_001371209.1:p.Glu157Asp
|
|
NM_001384290.1:c.456G>C
MANE Select
|
NP_001371219.1:p.Glu152Asp
|
|
NM_002127.6:c.456G>C
|
NP_002118.1:p.Glu152Asp
|
|