|
ENST00000361492.9:c.1342G>T
MANE Select
|
ENSP00000354586.5:p.Gly448Trp
|
|
|
ENST00000452319.6:c.1393G>T
|
ENSP00000390436.1:p.Gly465Trp
|
|
|
ENST00000314490.15:c.406G>T
|
ENSP00000312694.12:p.Gly136Trp
|
|
|
ENST00000341310.10:c.*441G>T
|
ENSP00000344473.6:n.*441G>T
|
|
|
ENST00000361492.8:c.1393G>T
|
ENSP00000354586.4:p.Gly465Trp
|
|
|
ENST00000435313.6:n.1367G>T
|
|
|
|
ENST00000437950.5:c.*492G>T
|
ENSP00000415773.1:n.*492G>T
|
|
|
ENST00000438299.5:c.*492G>T
|
ENSP00000400593.1:n.*492G>T
|
|
|
ENST00000445186.5:c.*492G>T
|
ENSP00000397488.1:n.*492G>T
|
|
|
ENST00000452319.5:c.1393G>T
|
ENSP00000390436.1:p.Gly465Trp
|
|
|
ENST00000452692.5:c.*441G>T
|
ENSP00000403715.1:n.*441G>T
|
|
|
NM_005270.4:c.1393G>T
|
NP_005261.2:p.Gly465Trp
|
|
|
XM_006712422.1:c.1342G>T
|
XP_006712485.1:p.Gly448Trp
|
|
|
XM_011510969.1:c.1375G>T
|
XP_011509271.1:p.Gly459Trp
|
|
|
XM_011510970.1:c.1252G>T
|
XP_011509272.1:p.Gly418Trp
|
|
|
XM_011510971.1:c.1198G>T
|
XP_011509273.1:p.Gly400Trp
|
|
|
XM_011510972.1:c.1198G>T
|
XP_011509274.1:p.Gly400Trp
|
|
|
XM_011510973.1:c.1018G>T
|
XP_011509275.1:p.Gly340Trp
|
|
|
XM_011510974.1:c.967G>T
|
XP_011509276.1:p.Gly323Trp
|
|
|
XM_006712422.3:c.1342G>T
|
XP_006712485.1:p.Gly448Trp
|
|
|
XM_011510969.2:c.1645G>T
|
XP_011509271.2:p.Gly549Trp
|
|
|
XM_011510970.2:c.1252G>T
|
XP_011509272.1:p.Gly418Trp
|
|
|
XM_011510971.2:c.1198G>T
|
XP_011509273.1:p.Gly400Trp
|
|
|
XM_011510972.2:c.1294G>T
|
XP_011509274.2:p.Gly432Trp
|
|
|
XM_011510973.2:c.1018G>T
|
XP_011509275.1:p.Gly340Trp
|
|
|
XM_011510974.2:c.967G>T
|
XP_011509276.1:p.Gly323Trp
|
|
|
XM_017003818.1:c.1594G>T
|
XP_016859307.1:p.Gly532Trp
|
|
|
XM_024452794.1:c.1393G>T
|
XP_024308562.1:p.Gly465Trp
|
|
|
XM_024452795.1:c.1393G>T
|
XP_024308563.1:p.Gly465Trp
|
|
|
NM_001371271.1:c.1393G>T
|
NP_001358200.1:p.Gly465Trp
|
|
|
NM_001374353.1:c.1342G>T
MANE Select
|
NP_001361282.1:p.Gly448Trp
|
|
|
NM_001374354.1:c.967G>T
|
NP_001361283.1:p.Gly323Trp
|
|
|
NM_005270.5:c.1393G>T
|
NP_005261.2:p.Gly465Trp
|
|
