|
ENST00000361492.9:c.3001G>T
MANE Select
|
ENSP00000354586.5:p.Gly1001Cys
|
|
|
ENST00000452319.6:c.3052G>T
|
ENSP00000390436.1:p.Gly1018Cys
|
|
|
ENST00000341310.10:c.*2100G>T
|
ENSP00000344473.6:n.*2100G>T
|
|
|
ENST00000361492.8:c.3052G>T
|
ENSP00000354586.4:p.Gly1018Cys
|
|
|
ENST00000438299.5:c.*2151G>T
|
ENSP00000400593.1:n.*2151G>T
|
|
|
ENST00000445186.5:c.*2151G>T
|
ENSP00000397488.1:n.*2151G>T
|
|
|
ENST00000452319.5:c.3052G>T
|
ENSP00000390436.1:p.Gly1018Cys
|
|
|
ENST00000452692.5:c.*2100G>T
|
ENSP00000403715.1:n.*2100G>T
|
|
|
NM_005270.4:c.3052G>T
|
NP_005261.2:p.Gly1018Cys
|
|
|
XM_006712422.1:c.3001G>T
|
XP_006712485.1:p.Gly1001Cys
|
|
|
XM_011510969.1:c.3034G>T
|
XP_011509271.1:p.Gly1012Cys
|
|
|
XM_011510970.1:c.2911G>T
|
XP_011509272.1:p.Gly971Cys
|
|
|
XM_011510971.1:c.2857G>T
|
XP_011509273.1:p.Gly953Cys
|
|
|
XM_011510972.1:c.2857G>T
|
XP_011509274.1:p.Gly953Cys
|
|
|
XM_011510973.1:c.2677G>T
|
XP_011509275.1:p.Gly893Cys
|
|
|
XM_011510974.1:c.2626G>T
|
XP_011509276.1:p.Gly876Cys
|
|
|
XM_006712422.3:c.3001G>T
|
XP_006712485.1:p.Gly1001Cys
|
|
|
XM_011510969.2:c.3304G>T
|
XP_011509271.2:p.Gly1102Cys
|
|
|
XM_011510970.2:c.2911G>T
|
XP_011509272.1:p.Gly971Cys
|
|
|
XM_011510971.2:c.2857G>T
|
XP_011509273.1:p.Gly953Cys
|
|
|
XM_011510972.2:c.2953G>T
|
XP_011509274.2:p.Gly985Cys
|
|
|
XM_011510973.2:c.2677G>T
|
XP_011509275.1:p.Gly893Cys
|
|
|
XM_011510974.2:c.2626G>T
|
XP_011509276.1:p.Gly876Cys
|
|
|
XM_017003818.1:c.3253G>T
|
XP_016859307.1:p.Gly1085Cys
|
|
|
XM_024452794.1:c.3052G>T
|
XP_024308562.1:p.Gly1018Cys
|
|
|
XM_024452795.1:c.3052G>T
|
XP_024308563.1:p.Gly1018Cys
|
|
|
NM_001371271.1:c.3052G>T
|
NP_001358200.1:p.Gly1018Cys
|
|
|
NM_001374353.1:c.3001G>T
MANE Select
|
NP_001361282.1:p.Gly1001Cys
|
|
|
NM_001374354.1:c.2626G>T
|
NP_001361283.1:p.Gly876Cys
|
|
|
NM_005270.5:c.3052G>T
|
NP_005261.2:p.Gly1018Cys
|
|
