ENST00000354393.7:c.3081A>C
|
ENSP00000346369.2:p.Glu1027Asp
|
|
ENST00000540630.6:c.3960A>C
|
ENSP00000441668.3:p.Glu1320Asp
|
|
ENST00000613327.5:c.3906A>C
|
ENSP00000480757.2:p.Glu1302Asp
|
|
ENST00000688812.1:c.*1169A>C
|
ENSP00000510658.1:n.*1169A>C
|
|
ENST00000690544.1:c.*3177A>C
|
ENSP00000508989.1:n.*3177A>C
|
|
ENST00000358913.10:c.3906A>C
MANE Select
|
ENSP00000351790.5:p.Glu1302Asp
|
|
ENST00000354393.6:c.3081A>C
|
ENSP00000346369.2:p.Glu1027Asp
|
|
ENST00000358913.9:c.3906A>C
|
ENSP00000351790.5:p.Glu1302Asp
|
|
ENST00000540630.5:c.3906A>C
|
ENSP00000441668.2:p.Glu1302Asp
|
|
ENST00000613327.4:c.3024A>C
|
ENSP00000480757.1:p.Glu1008Asp
|
|
NM_001256267.1:c.3906A>C
|
NP_001243196.1:p.Glu1302Asp
|
|
NM_001256268.1:c.3024A>C
|
NP_001243197.1:p.Glu1008Asp
|
|
NM_032578.3:c.3906A>C , LRG_410t1:c.3906A>C
|
NP_115967.2:p.Glu1302Asp
|
|
NR_045662.3:n.3333A>C
|
|
|
NR_045663.3:n.4035A>C
|
|
|
XM_006718043.2:c.3960A>C
|
XP_006718106.1:p.Glu1320Asp
|
|
XM_011540292.1:c.3936A>C
|
XP_011538594.1:p.Glu1312Asp
|
|
XR_946029.1:n.1574+4890T>G
|
|
|
XM_017016833.1:c.3984A>C
|
XP_016872322.1:p.Glu1328Asp
|
|
XM_017016834.2:c.3906A>C
|
XP_016872323.1:p.Glu1302Asp
|
|
XM_024448236.1:c.2784A>C
|
XP_024304004.1:p.Glu928Asp
|
|
NR_045662.4:n.3443A>C
|
|
|
NR_045663.4:n.3980A>C
|
|
|
NM_001256267.2:c.3906A>C
|
NP_001243196.1:p.Glu1302Asp
|
|
NM_001256268.2:c.3024A>C
|
NP_001243197.1:p.Glu1008Asp
|
|
NM_032578.4:c.3906A>C
MANE Select
|
NP_115967.2:p.Glu1302Asp
|
|