ENST00000013070.11:c.611T>G
MANE Select
|
ENSP00000013070.6:p.Ile204Arg
|
|
ENST00000013070.10:c.611T>G
|
ENSP00000013070.6:p.Ile204Arg
|
|
ENST00000416753.5:c.383T>G
|
ENSP00000391706.2:p.Ile128Arg
|
|
ENST00000553674.1:c.*312T>G
|
ENSP00000450470.1:n.*312T>G
|
|
ENST00000553857.5:c.378+3255T>G
|
|
|
ENST00000554232.5:c.515T>G
|
ENSP00000450645.1:p.Ile172Arg
|
|
ENST00000556871.5:c.320T>G
|
ENSP00000451022.1:p.Ile107Arg
|
|
ENST00000557048.1:n.520T>G
|
|
|
NM_175748.3:c.611T>G
|
NP_786924.2:p.Ile204Arg
|
|
NR_038150.1:n.713T>G
|
|
|
NM_175748.4:c.611T>G
MANE Select
|
NP_786924.2:p.Ile204Arg
|
|
NR_038150.2:n.513T>G
|
|
|