ENST00000391944.8:c.2146G=
|
ENSP00000375808.4:p.Val716=
|
|
ENST00000682414.1:c.2146G=
|
ENSP00000507019.1:p.Val716=
|
|
ENST00000682508.1:n.2175G=
|
|
|
ENST00000684218.1:c.*1404G=
|
ENSP00000507804.1:n.*1404G=
|
|
ENST00000684264.1:n.1702G=
|
|
|
ENST00000684407.1:c.2023G=
|
ENSP00000507775.1:p.Val675=
|
|
ENST00000684458.1:c.*632G=
|
ENSP00000508260.1:n.*632G=
|
|
ENST00000684468.1:n.1858G=
|
|
|
ENST00000391945.10:c.2146G=
MANE Select
|
ENSP00000375809.4:p.Val716=
|
|
ENST00000646507.1:n.2243G=
|
|
|
ENST00000391941.6:c.2074G=
|
ENSP00000375805.2:p.Val692=
|
|
ENST00000391942.6:n.1317G=
|
|
|
ENST00000391944.7:c.1912G=
|
ENSP00000375808.3:p.Val638=
|
|
ENST00000391945.8:c.2146G=
|
ENSP00000375809.3:p.Val716=
|
|
ENST00000588652.5:n.2234G=
|
|
|
NM_000400.3:c.2146G= , LRG_461t1:c.2146G=
|
NP_000391.1:p.Val716=
|
|
XM_011526611.1:c.2068G=
|
XP_011524913.1:p.Val690=
|
|
XM_011526611.2:c.2068G=
|
XP_011524913.1:p.Val690=
|
|
XM_017026467.1:c.2023G=
|
XP_016881956.1:p.Val675=
|
|
XR_001753633.2:n.2193G=
|
|
|
XR_001753634.2:n.2129G=
|
|
|
NM_000400.4:c.2146G=
MANE Select
|
NP_000391.1:p.Val716=
|
|