ENST00000295897.9:c.514T>C
MANE Select
|
ENSP00000295897.4:p.Tyr172His
|
|
ENST00000295897.8:c.514T>C
|
ENSP00000295897.4:p.Tyr172His
|
|
ENST00000401494.7:c.169T>C
|
ENSP00000384695.3:p.Tyr57His
|
|
ENST00000415165.6:c.138-2610T>C
|
ENSP00000401820.2:n.138-2610T>C
|
|
ENST00000441319.5:c.520T>C
|
ENSP00000392541.1:p.Tyr174His
|
|
ENST00000476441.6:c.111T>C
|
ENSP00000423727.1:p.Leu37=
|
|
ENST00000503124.5:c.64T>C
|
ENSP00000421027.1:p.Tyr22His
|
|
ENST00000505649.5:n.200T>C
|
|
|
ENST00000509063.5:c.514T>C
|
ENSP00000422784.1:p.Tyr172His
|
|
ENST00000511370.1:c.47T>C
|
|
|
ENST00000514786.1:n.483T>C
|
|
|
ENST00000621085.4:c.490+24T>C
|
ENSP00000483421.1:n.490+24T>C
|
|
ENST00000621628.4:c.486+310T>C
|
ENSP00000480485.1:n.486+310T>C
|
|
NM_000477.5:c.514T>C
|
NP_000468.1:p.Tyr172His
|
|
NM_000477.6:c.514T>C
|
NP_000468.1:p.Tyr172His
|
|
NM_000477.7:c.514T>C
MANE Select
|
NP_000468.1:p.Tyr172His
|
|