ENST00000463045.3:c.295T>C
|
ENSP00000481376.2:p.Tyr99His
|
|
ENST00000491274.6:c.424T>C
|
ENSP00000480482.2:p.Tyr142His
|
|
ENST00000375499.8:c.466T>C
MANE Select
|
ENSP00000364649.3:p.Tyr156His
|
|
ENST00000375499.7:c.466T>C
|
ENSP00000364649.3:p.Tyr156His
|
|
ENST00000463045.2:c.295T>C
|
ENSP00000481376.1:p.Tyr99His
|
|
ENST00000475506.1:n.383T>C
|
|
|
ENST00000485515.5:n.400T>C
|
|
|
ENST00000491274.5:c.424T>C
|
ENSP00000480482.1:p.Tyr142His
|
|
NM_003000.2:c.466T>C , LRG_316t1:c.466T>C
|
NP_002991.2:p.Tyr156His
|
|
NM_003000.3:c.466T>C
MANE Select
|
NP_002991.2:p.Tyr156His
|
|