ENST00000350721.9:c.6304T>C
MANE Select
|
ENSP00000343741.4:p.Tyr2102His
|
|
ENST00000513291.2:n.1488T>C
|
|
|
ENST00000654170.1:n.1147T>C
|
|
|
ENST00000656590.1:c.5094T>C
|
|
|
ENST00000661310.1:c.6112T>C
|
ENSP00000499589.1:p.Tyr2038His
|
|
ENST00000665483.1:n.159T>C
|
|
|
ENST00000666447.1:n.139T>C
|
|
|
ENST00000666943.1:n.1768T>C
|
|
|
ENST00000350721.8:c.6304T>C
|
ENSP00000343741.4:p.Tyr2102His
|
|
NM_001184.3:c.6304T>C
|
NP_001175.2:p.Tyr2102His
|
|
XM_011512924.1:c.6310T>C
|
XP_011511226.1:p.Tyr2104His
|
|
XM_011512925.1:c.6118T>C
|
XP_011511227.1:p.Tyr2040His
|
|
XR_924147.1:n.6399T>C
|
|
|
XR_924148.1:n.6399T>C
|
|
|
XR_924149.1:n.6278T>C
|
|
|
NM_001354579.1:c.6112T>C
|
NP_001341508.1:p.Tyr2038His
|
|
XR_001740179.2:n.6393T>C
|
|
|
XR_001740180.2:n.6447T>C
|
|
|
XR_001740181.2:n.6326T>C
|
|
|
XR_001740182.1:n.6278T>C
|
|
|
XR_002959543.1:n.6503T>C
|
|
|
XR_924148.2:n.6399T>C
|
|
|
NM_001184.4:c.6304T>C
MANE Select
|
NP_001175.2:p.Tyr2102His
|
|
NM_001354579.2:c.6112T>C
|
NP_001341508.1:p.Tyr2038His
|
|