ENST00000317961.9:c.3620T>A
MANE Select
|
ENSP00000322408.4:p.Leu1207His
|
|
ENST00000317961.8:c.3620T>A
|
ENSP00000322408.4:p.Leu1207His
|
|
ENST00000382806.6:c.3449T>A
|
ENSP00000372256.2:p.Leu1150His
|
|
ENST00000415360.1:c.536T>A
|
ENSP00000389433.1:p.Leu179His
|
|
ENST00000440077.5:c.3497T>A
|
ENSP00000398543.1:p.Leu1166His
|
|
ENST00000469599.6:n.2218T>A
|
|
|
ENST00000492117.1:n.3512T>A
|
|
|
ENST00000541639.5:c.3713T>A
|
ENSP00000444293.1:p.Leu1238His
|
|
NM_001146705.1:c.3713T>A
|
NP_001140177.1:p.Leu1238His
|
|
NM_001146706.1:c.3449T>A
|
NP_001140178.1:p.Leu1150His
|
|
NM_004653.4:c.3620T>A
|
NP_004644.2:p.Leu1207His
|
|
XM_005262560.1:c.3485T>A
|
XP_005262617.1:p.Leu1162His
|
|
XM_005262561.1:c.3389T>A
|
XP_005262618.1:p.Leu1130His
|
|
XM_011531468.1:c.3542T>A
|
XP_011529770.1:p.Leu1181His
|
|
XR_244571.2:n.3908T>A
|
|
|
XR_430568.2:n.4242T>A
|
|
|
XM_005262560.3:c.3485T>A
|
XP_005262617.1:p.Leu1162His
|
|
XM_005262561.3:c.3389T>A
|
XP_005262618.1:p.Leu1130His
|
|
XM_011531468.3:c.3542T>A
|
XP_011529770.1:p.Leu1181His
|
|
XM_024452495.1:c.1610T>A
|
XP_024308263.1:p.Leu537His
|
|
XM_024452496.1:c.1376T>A
|
XP_024308264.1:p.Leu459His
|
|
XR_001756009.2:n.4358T>A
|
|
|
XR_001756010.2:n.4358T>A
|
|
|
XR_001756011.2:n.4223T>A
|
|
|
XR_001756012.2:n.4371T>A
|
|
|
XR_001756013.2:n.3689T>A
|
|
|
XR_002958832.1:n.3790T>A
|
|
|
XR_002958834.1:n.4014T>A
|
|
|
XR_002958835.1:n.3897T>A
|
|
|
XR_002958836.1:n.4580T>A
|
|
|
XR_002958837.1:n.4387T>A
|
|
|
XR_244571.4:n.3907T>A
|
|
|
XR_430568.4:n.4241T>A
|
|
|
NM_001146706.2:c.3449T>A
|
NP_001140178.1:p.Leu1150His
|
|
NM_004653.5:c.3620T>A
MANE Select
|
NP_004644.2:p.Leu1207His
|
|
NM_001146705.2:c.3713T>A
|
NP_001140177.1:p.Leu1238His
|
|