ENST00000317961.9:c.3333G>T
MANE Select
|
ENSP00000322408.4:p.Gly1111=
|
|
ENST00000317961.8:c.3333G>T
|
ENSP00000322408.4:p.Gly1111=
|
|
ENST00000382806.6:c.3162G>T
|
ENSP00000372256.2:p.Gly1054=
|
|
ENST00000415360.1:c.249G>T
|
ENSP00000389433.1:p.Gly83=
|
|
ENST00000440077.5:c.3210G>T
|
ENSP00000398543.1:p.Gly1070=
|
|
ENST00000469599.6:n.1931G>T
|
|
|
ENST00000492117.1:n.3225G>T
|
|
|
ENST00000541639.5:c.3426G>T
|
ENSP00000444293.1:p.Gly1142=
|
|
NM_001146705.1:c.3426G>T
|
NP_001140177.1:p.Gly1142=
|
|
NM_001146706.1:c.3162G>T
|
NP_001140178.1:p.Gly1054=
|
|
NM_004653.4:c.3333G>T
|
NP_004644.2:p.Gly1111=
|
|
XM_005262560.1:c.3198G>T
|
XP_005262617.1:p.Gly1066=
|
|
XM_005262561.1:c.3102G>T
|
XP_005262618.1:p.Gly1034=
|
|
XM_011531468.1:c.3255G>T
|
XP_011529770.1:p.Gly1085=
|
|
XR_244571.2:n.3621G>T
|
|
|
XR_430568.2:n.3955G>T
|
|
|
XM_005262560.3:c.3198G>T
|
XP_005262617.1:p.Gly1066=
|
|
XM_005262561.3:c.3102G>T
|
XP_005262618.1:p.Gly1034=
|
|
XM_011531468.3:c.3255G>T
|
XP_011529770.1:p.Gly1085=
|
|
XM_024452495.1:c.1323G>T
|
XP_024308263.1:p.Gly441=
|
|
XM_024452496.1:c.1089G>T
|
XP_024308264.1:p.Gly363=
|
|
XR_001756009.2:n.4071G>T
|
|
|
XR_001756010.2:n.4071G>T
|
|
|
XR_001756011.2:n.3936G>T
|
|
|
XR_001756012.2:n.4084G>T
|
|
|
XR_001756013.2:n.3402G>T
|
|
|
XR_002958832.1:n.3503G>T
|
|
|
XR_002958834.1:n.3727G>T
|
|
|
XR_002958835.1:n.3610G>T
|
|
|
XR_002958836.1:n.4293G>T
|
|
|
XR_002958837.1:n.4100G>T
|
|
|
XR_244571.4:n.3620G>T
|
|
|
XR_430568.4:n.3954G>T
|
|
|
NM_001146706.2:c.3162G>T
|
NP_001140178.1:p.Gly1054=
|
|
NM_004653.5:c.3333G>T
MANE Select
|
NP_004644.2:p.Gly1111=
|
|
NM_001146705.2:c.3426G>T
|
NP_001140177.1:p.Gly1142=
|
|