ENST00000354393.7:c.1076G>T
|
ENSP00000346369.2:p.Gly359Val
|
|
ENST00000373675.4:c.1901G>T
|
ENSP00000362779.4:p.Gly634Val
|
|
ENST00000540630.6:c.1955G>T
|
ENSP00000441668.3:p.Gly652Val
|
|
ENST00000613327.5:c.1901G>T
|
ENSP00000480757.2:p.Gly634Val
|
|
ENST00000687572.1:c.779G>T
|
ENSP00000510427.1:p.Gly260Val
|
|
ENST00000688812.1:c.1877G>T
|
ENSP00000510658.1:p.Gly626Val
|
|
ENST00000690544.1:c.*1172G>T
|
ENSP00000508989.1:n.*1172G>T
|
|
ENST00000358913.10:c.1901G>T
MANE Select
|
ENSP00000351790.5:p.Gly634Val
|
|
ENST00000354393.6:c.1076G>T
|
ENSP00000346369.2:p.Gly359Val
|
|
ENST00000358913.9:c.1901G>T
|
ENSP00000351790.5:p.Gly634Val
|
|
ENST00000540630.5:c.1901G>T
|
ENSP00000441668.2:p.Gly634Val
|
|
ENST00000613327.4:c.1019G>T
|
ENSP00000480757.1:p.Gly340Val
|
|
NM_001256267.1:c.1901G>T
|
NP_001243196.1:p.Gly634Val
|
|
NM_001256268.1:c.1019G>T
|
NP_001243197.1:p.Gly340Val
|
|
NM_032578.3:c.1901G>T , LRG_410t1:c.1901G>T
|
NP_115967.2:p.Gly634Val
|
|
NR_045662.3:n.1328G>T
|
|
|
NR_045663.3:n.2169G>T
|
|
|
XM_006718043.2:c.1955G>T
|
XP_006718106.1:p.Gly652Val
|
|
XM_011540292.1:c.1931G>T
|
XP_011538594.1:p.Gly644Val
|
|
XM_017016833.1:c.1979G>T
|
XP_016872322.1:p.Gly660Val
|
|
XM_017016834.2:c.1901G>T
|
XP_016872323.1:p.Gly634Val
|
|
XM_024448236.1:c.779G>T
|
XP_024304004.1:p.Gly260Val
|
|
NR_045662.4:n.1438G>T
|
|
|
NR_045663.4:n.2114G>T
|
|
|
NM_001256267.2:c.1901G>T
|
NP_001243196.1:p.Gly634Val
|
|
NM_001256268.2:c.1019G>T
|
NP_001243197.1:p.Gly340Val
|
|
NM_032578.4:c.1901G>T
MANE Select
|
NP_115967.2:p.Gly634Val
|
|