ENST00000703783.1:n.1126T>G
|
|
|
ENST00000703785.1:n.1207T>G
|
|
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ENST00000262464.9:c.4342T>G
MANE Select
|
ENSP00000262464.4:p.Ser1448Ala
|
|
ENST00000262464.8:c.4342T>G
|
ENSP00000262464.4:p.Ser1448Ala
|
|
ENST00000507835.5:c.892T>G
|
ENSP00000426839.1:p.Ser298Ala
|
|
ENST00000508053.5:c.4342T>G
|
ENSP00000424571.1:p.Ser1448Ala
|
|
ENST00000508989.5:c.4243T>G
|
ENSP00000425596.1:p.Ser1415Ala
|
|
ENST00000619499.4:c.4339T>G
|
ENSP00000482132.1:p.Ser1447Ala
|
|
NM_001999.3:c.4342T>G
|
NP_001990.2:p.Ser1448Ala
|
|
XM_017009228.2:c.4189T>G
|
XP_016864717.1:p.Ser1397Ala
|
|
NM_001999.4:c.4342T>G
MANE Select
|
NP_001990.2:p.Ser1448Ala
|
|