ENST00000354393.7:c.661G>T
|
ENSP00000346369.2:p.Glu221Ter
|
|
ENST00000373675.4:c.1486G>T
|
ENSP00000362779.4:p.Glu496Ter
|
|
ENST00000540630.6:c.1540G>T
|
ENSP00000441668.3:p.Glu514Ter
|
|
ENST00000613327.5:c.1486G>T
|
ENSP00000480757.2:p.Glu496Ter
|
|
ENST00000687572.1:c.364G>T
|
ENSP00000510427.1:p.Glu122Ter
|
|
ENST00000687705.1:c.*1735G>T
|
ENSP00000509639.1:n.*1735G>T
|
|
ENST00000688812.1:c.1462G>T
|
ENSP00000510658.1:p.Glu488Ter
|
|
ENST00000689002.1:n.538G>T
|
|
|
ENST00000690544.1:c.*757G>T
|
ENSP00000508989.1:n.*757G>T
|
|
ENST00000358913.10:c.1486G>T
MANE Select
|
ENSP00000351790.5:p.Glu496Ter
|
|
ENST00000354393.6:c.661G>T
|
ENSP00000346369.2:p.Glu221Ter
|
|
ENST00000358913.9:c.1486G>T
|
ENSP00000351790.5:p.Glu496Ter
|
|
ENST00000540630.5:c.1486G>T
|
ENSP00000441668.2:p.Glu496Ter
|
|
ENST00000613327.4:c.604G>T
|
ENSP00000480757.1:p.Glu202Ter
|
|
NM_001256267.1:c.1486G>T
|
NP_001243196.1:p.Glu496Ter
|
|
NM_001256268.1:c.604G>T
|
NP_001243197.1:p.Glu202Ter
|
|
NM_032578.3:c.1486G>T , LRG_410t1:c.1486G>T
|
NP_115967.2:p.Glu496Ter
|
|
NR_045662.3:n.913G>T
|
|
|
NR_045663.3:n.1754G>T
|
|
|
XM_006718043.2:c.1540G>T
|
XP_006718106.1:p.Glu514Ter
|
|
XM_011540292.1:c.1516G>T
|
XP_011538594.1:p.Glu506Ter
|
|
XM_017016833.1:c.1564G>T
|
XP_016872322.1:p.Glu522Ter
|
|
XM_017016834.2:c.1486G>T
|
XP_016872323.1:p.Glu496Ter
|
|
XM_024448236.1:c.364G>T
|
XP_024304004.1:p.Glu122Ter
|
|
NR_045662.4:n.1023G>T
|
|
|
NR_045663.4:n.1699G>T
|
|
|
NM_001256267.2:c.1486G>T
|
NP_001243196.1:p.Glu496Ter
|
|
NM_001256268.2:c.604G>T
|
NP_001243197.1:p.Glu202Ter
|
|
NM_032578.4:c.1486G>T
MANE Select
|
NP_115967.2:p.Glu496Ter
|
|