ENST00000295897.9:c.602G>A
MANE Select
|
ENSP00000295897.4:p.Cys201Tyr
|
|
ENST00000295897.8:c.602G>A
|
ENSP00000295897.4:p.Cys201Tyr
|
|
ENST00000401494.7:c.257G>A
|
ENSP00000384695.3:p.Cys86Tyr
|
|
ENST00000415165.6:c.138-2522G>A
|
ENSP00000401820.2:n.138-2522G>A
|
|
ENST00000476441.6:c.199G>A
|
ENSP00000423727.1:p.Ala67Thr
|
|
ENST00000503124.5:c.152G>A
|
ENSP00000421027.1:p.Cys51Tyr
|
|
ENST00000505649.5:n.288G>A
|
|
|
ENST00000509063.5:c.602G>A
|
ENSP00000422784.1:p.Cys201Tyr
|
|
ENST00000511370.1:c.135G>A
|
|
|
ENST00000514786.1:n.571G>A
|
|
|
ENST00000621085.4:c.490+112G>A
|
ENSP00000483421.1:n.490+112G>A
|
|
ENST00000621628.4:c.486+398G>A
|
ENSP00000480485.1:n.486+398G>A
|
|
NM_000477.5:c.602G>A
|
NP_000468.1:p.Cys201Tyr
|
|
NM_000477.6:c.602G>A
|
NP_000468.1:p.Cys201Tyr
|
|
NM_000477.7:c.602G>A
MANE Select
|
NP_000468.1:p.Cys201Tyr
|
|