ENST00000703783.1:n.1083C>G
|
|
|
ENST00000703785.1:n.1164C>G
|
|
|
ENST00000262464.9:c.4299C>G
MANE Select
|
ENSP00000262464.4:p.Arg1433=
|
|
ENST00000262464.8:c.4299C>G
|
ENSP00000262464.4:p.Arg1433=
|
|
ENST00000507835.5:c.849C>G
|
ENSP00000426839.1:p.Arg283=
|
|
ENST00000508053.5:c.4299C>G
|
ENSP00000424571.1:p.Arg1433=
|
|
ENST00000508989.5:c.4200C>G
|
ENSP00000425596.1:p.Arg1400=
|
|
ENST00000619499.4:c.4296C>G
|
ENSP00000482132.1:p.Arg1432=
|
|
NM_001999.3:c.4299C>G
|
NP_001990.2:p.Arg1433=
|
|
XM_017009228.2:c.4146C>G
|
XP_016864717.1:p.Arg1382=
|
|
NM_001999.4:c.4299C>G
MANE Select
|
NP_001990.2:p.Arg1433=
|
|