ENST00000477226.6:n.881G=
|
|
|
ENST00000683013.1:n.795G=
|
|
|
ENST00000373960.4:c.1407G=
MANE Select
|
ENSP00000363071.3:p.Val469=
|
|
ENST00000373960.3:c.1407G=
|
ENSP00000363071.3:p.Val469=
|
|
ENST00000483395.1:n.262G=
|
|
|
NM_001927.3:c.1407G= , LRG_380t1:c.1407G=
|
NP_001918.3:p.Val469=
|
|
NM_001927.4:c.1407G=
MANE Select
|
NP_001918.3:p.Val469=
|
|
NM_001382708.1:c.1404G=
|
NP_001369637.1:p.Val468=
|
|
NM_001382709.1:c.975G=
|
NP_001369638.1:p.Val325=
|
|
NM_001382710.1:c.1338G=
|
NP_001369639.1:p.Val446=
|
|
NM_001382711.1:c.1386G=
|
NP_001369640.1:p.Val462=
|
|
NM_001382712.1:c.1371+239G=
|
NP_001369641.1:n.1371+239G=
|
|
NM_001382713.1:c.1137G=
|
NP_001369642.1:p.Val379=
|
|