ENST00000391944.8:c.2129T>C
|
ENSP00000375808.4:p.Val710Ala
|
|
ENST00000682414.1:c.2129T>C
|
ENSP00000507019.1:p.Val710Ala
|
|
ENST00000682508.1:n.2158T>C
|
|
|
ENST00000684218.1:c.*1387T>C
|
ENSP00000507804.1:n.*1387T>C
|
|
ENST00000684264.1:n.1685T>C
|
|
|
ENST00000684407.1:c.2006T>C
|
ENSP00000507775.1:p.Val669Ala
|
|
ENST00000684458.1:c.*615T>C
|
ENSP00000508260.1:n.*615T>C
|
|
ENST00000684468.1:n.1841T>C
|
|
|
ENST00000391945.10:c.2129T>C
MANE Select
|
ENSP00000375809.4:p.Val710Ala
|
|
ENST00000646507.1:n.2226T>C
|
|
|
ENST00000391941.6:c.2057T>C
|
ENSP00000375805.2:p.Val686Ala
|
|
ENST00000391942.6:n.1300T>C
|
|
|
ENST00000391944.7:c.1895T>C
|
ENSP00000375808.3:p.Val632Ala
|
|
ENST00000391945.8:c.2129T>C
|
ENSP00000375809.3:p.Val710Ala
|
|
ENST00000588652.5:n.2217T>C
|
|
|
NM_000400.3:c.2129T>C , LRG_461t1:c.2129T>C
|
NP_000391.1:p.Val710Ala
|
|
XM_011526611.1:c.2051T>C
|
XP_011524913.1:p.Val684Ala
|
|
XM_011526611.2:c.2051T>C
|
XP_011524913.1:p.Val684Ala
|
|
XM_017026467.1:c.2006T>C
|
XP_016881956.1:p.Val669Ala
|
|
XR_001753633.2:n.2176T>C
|
|
|
XR_001753634.2:n.2112T>C
|
|
|
NM_000400.4:c.2129T>C
MANE Select
|
NP_000391.1:p.Val710Ala
|
|