ENST00000428701.6:n.522-9T>C
|
|
|
ENST00000360323.11:c.409T>C
MANE Select
|
ENSP00000353472.6:p.Tyr137His
|
|
ENST00000360323.10:c.409T>C
|
ENSP00000353472.6:p.Tyr137His
|
|
ENST00000376815.3:c.343+292T>C
|
ENSP00000366011.3:n.343+292T>C
|
|
ENST00000376818.7:c.343+292T>C
|
ENSP00000366014.3:n.343+292T>C
|
|
ENST00000376828.6:c.424T>C
|
ENSP00000366024.2:p.Tyr142His
|
|
ENST00000428701.5:c.409T>C
|
ENSP00000412927.1:p.Tyr137His
|
|
ENST00000478355.5:n.409T>C
|
|
|
ENST00000478519.5:c.343+292T>C
|
ENSP00000436375.1:n.343+292T>C
|
|
NM_002127.5:c.409T>C
|
NP_002118.1:p.Tyr137His
|
|
NM_001363567.1:c.424T>C
|
NP_001350496.1:p.Tyr142His
|
|
XM_017010817.1:c.343+292T>C
|
XP_016866306.1:n.343+292T>C
|
|
XM_017010818.1:c.343+292T>C
|
XP_016866307.1:n.343+292T>C
|
|
XM_024446420.1:c.409T>C
|
XP_024302188.1:p.Tyr137His
|
|
NM_001363567.2:c.424T>C
|
NP_001350496.1:p.Tyr142His
|
|
NM_001384280.1:c.424T>C
|
NP_001371209.1:p.Tyr142His
|
|
NM_001384290.1:c.409T>C
MANE Select
|
NP_001371219.1:p.Tyr137His
|
|
NM_002127.6:c.409T>C
|
NP_002118.1:p.Tyr137His
|
|