ENST00000264595.7:c.422T>A
MANE Select
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ENSP00000264595.2:p.Phe141Tyr
|
|
ENST00000264595.6:c.422T>A
|
ENSP00000264595.2:p.Phe141Tyr
|
|
ENST00000502310.5:c.77T>A
|
ENSP00000423798.1:p.Phe26Tyr
|
|
ENST00000506853.5:n.456T>A
|
|
|
ENST00000510635.1:c.118T>A
|
|
|
ENST00000510955.5:n.343T>A
|
|
|
NM_000027.3:c.422T>A
|
NP_000018.2:p.Phe141Tyr
|
|
NM_001171988.1:c.422T>A
|
NP_001165459.1:p.Phe141Tyr
|
|
NR_033655.1:n.550T>A
|
|
|
XM_006714123.2:c.422T>A
|
XP_006714186.1:p.Phe141Tyr
|
|
XR_001741155.2:n.516T>A
|
|
|
NM_000027.4:c.422T>A
MANE Select
|
NP_000018.2:p.Phe141Tyr
|
|
NM_001171988.2:c.422T>A
|
NP_001165459.1:p.Phe141Tyr
|
|
NR_033655.2:n.484T>A
|
|
|