ENST00000391944.8:c.2141T>A
|
ENSP00000375808.4:p.Val714Asp
|
|
ENST00000682414.1:c.2141T>A
|
ENSP00000507019.1:p.Val714Asp
|
|
ENST00000682508.1:n.2170T>A
|
|
|
ENST00000684218.1:c.*1399T>A
|
ENSP00000507804.1:n.*1399T>A
|
|
ENST00000684264.1:n.1697T>A
|
|
|
ENST00000684407.1:c.2018T>A
|
ENSP00000507775.1:p.Val673Asp
|
|
ENST00000684458.1:c.*627T>A
|
ENSP00000508260.1:n.*627T>A
|
|
ENST00000684468.1:n.1853T>A
|
|
|
ENST00000391945.10:c.2141T>A
MANE Select
|
ENSP00000375809.4:p.Val714Asp
|
|
ENST00000646507.1:n.2238T>A
|
|
|
ENST00000391941.6:c.2069T>A
|
ENSP00000375805.2:p.Val690Asp
|
|
ENST00000391942.6:n.1312T>A
|
|
|
ENST00000391944.7:c.1907T>A
|
ENSP00000375808.3:p.Val636Asp
|
|
ENST00000391945.8:c.2141T>A
|
ENSP00000375809.3:p.Val714Asp
|
|
ENST00000588652.5:n.2229T>A
|
|
|
NM_000400.3:c.2141T>A , LRG_461t1:c.2141T>A
|
NP_000391.1:p.Val714Asp
|
|
XM_011526611.1:c.2063T>A
|
XP_011524913.1:p.Val688Asp
|
|
XM_011526611.2:c.2063T>A
|
XP_011524913.1:p.Val688Asp
|
|
XM_017026467.1:c.2018T>A
|
XP_016881956.1:p.Val673Asp
|
|
XR_001753633.2:n.2188T>A
|
|
|
XR_001753634.2:n.2124T>A
|
|
|
NM_000400.4:c.2141T>A
MANE Select
|
NP_000391.1:p.Val714Asp
|
|