|
ENST00000473665.2:n.5233T>C
|
|
|
|
ENST00000482662.2:n.3640T>C
|
|
|
|
ENST00000685865.1:n.1592T>C
|
|
|
|
ENST00000687250.1:n.1292T>C
|
|
|
|
ENST00000687995.1:n.1541T>C
|
|
|
|
ENST00000688205.1:c.*782T>C
|
ENSP00000509673.1:n.*782T>C
|
|
|
ENST00000688788.1:n.1428T>C
|
|
|
|
ENST00000689276.1:c.1120T>C
|
ENSP00000510012.1:p.Tyr374His
|
|
|
ENST00000689576.1:c.1189T>C
|
ENSP00000508712.1:p.Tyr397His
|
|
|
ENST00000690108.1:c.*845T>C
|
ENSP00000510617.1:n.*845T>C
|
|
|
ENST00000690468.1:c.910T>C
|
ENSP00000509078.1:p.Tyr304His
|
|
|
ENST00000690595.1:c.514T>C
|
ENSP00000508979.1:p.Tyr172His
|
|
|
ENST00000691348.1:c.1018T>C
|
ENSP00000509369.1:p.Tyr340His
|
|
|
ENST00000691410.1:c.*766T>C
|
ENSP00000508479.1:n.*766T>C
|
|
|
ENST00000693287.1:c.505T>C
|
ENSP00000510264.1:p.Tyr169His
|
|
|
ENST00000693681.1:c.502T>C
|
ENSP00000510789.1:p.Tyr168His
|
|
|
ENST00000233838.9:c.1189T>C
MANE Select
|
ENSP00000233838.3:p.Tyr397His
|
|
|
ENST00000233838.8:c.1189T>C
|
ENSP00000233838.3:p.Tyr397His
|
|
|
ENST00000430215.7:c.1018T>C
|
ENSP00000408045.3:p.Tyr340His
|
|
|
ENST00000465637.5:n.179-5033T>C
|
|
|
|
ENST00000473665.1:n.682T>C
|
|
|
|
ENST00000482662.1:n.606T>C
|
|
|
|
NM_000821.5:c.1189T>C
|
NP_000812.2:p.Tyr397His
|
|
|
NM_000821.6:c.1189T>C
|
NP_000812.2:p.Tyr397His
|
|
|
NM_001142269.2:c.1018T>C
|
NP_001135741.1:p.Tyr340His
|
|
|
NM_001142269.3:c.1018T>C
|
NP_001135741.1:p.Tyr340His
|
|
|
XM_005264259.3:c.1189T>C
|
XP_005264316.1:p.Tyr397His
|
|
|
XM_011532764.1:c.367T>C
|
XP_011531066.1:p.Tyr123His
|
|
|
XM_011532765.1:c.367T>C
|
XP_011531067.1:p.Tyr123His
|
|
|
XR_939677.1:n.1254T>C
|
|
|
|
XM_005264259.5:c.1189T>C
|
XP_005264316.1:p.Tyr397His
|
|
|
XM_011532764.3:c.367T>C
|
XP_011531066.1:p.Tyr123His
|
|
|
XM_011532765.3:c.367T>C
|
XP_011531067.1:p.Tyr123His
|
|
|
XM_017003803.2:c.1018T>C
|
XP_016859292.1:p.Tyr340His
|
|
|
XR_001738703.2:n.1254T>C
|
|
|
|
NM_000821.7:c.1189T>C
MANE Select
|
NP_000812.2:p.Tyr397His
|
|
|
NM_001142269.4:c.1018T>C
|
NP_001135741.1:p.Tyr340His
|
|
