ENST00000269228.10:c.3636G>C
MANE Select
|
ENSP00000269228.4:p.Val1212=
|
|
ENST00000269228.9:c.3636G>C
|
ENSP00000269228.4:p.Val1212=
|
|
ENST00000586150.5:c.391G>C
|
|
|
ENST00000587163.1:n.160G>C
|
|
|
ENST00000588867.1:n.1319G>C
|
|
|
ENST00000590723.5:c.45G>C
|
ENSP00000464755.1:p.Val15=
|
|
ENST00000591051.1:c.2714G>C
|
|
|
ENST00000591107.6:c.313G>C
|
|
|
NM_000271.4:c.3636G>C
|
NP_000262.2:p.Val1212=
|
|
XM_005258277.1:c.3687G>C
|
XP_005258334.1:p.Val1229=
|
|
XM_005258278.3:c.3687G>C
|
XP_005258335.1:p.Val1229=
|
|
XM_005258279.1:c.3636G>C
|
XP_005258336.1:p.Val1212=
|
|
XM_006722479.2:c.3687G>C
|
XP_006722542.1:p.Val1229=
|
|
XM_011526015.1:c.3222G>C
|
XP_011524317.1:p.Val1074=
|
|
XM_005258278.5:c.3687G>C
|
XP_005258335.1:p.Val1229=
|
|
XM_005258279.2:c.3636G>C
|
XP_005258336.1:p.Val1212=
|
|
XM_006722479.3:c.3687G>C
|
XP_006722542.1:p.Val1229=
|
|
XM_017025784.1:c.3687G>C
|
XP_016881273.1:p.Val1229=
|
|
XM_017025785.1:c.3687G>C
|
XP_016881274.1:p.Val1229=
|
|
XM_017025786.1:c.3636G>C
|
XP_016881275.1:p.Val1212=
|
|
XM_017025787.1:c.3636G>C
|
XP_016881276.1:p.Val1212=
|
|
NM_000271.5:c.3636G>C
MANE Select
|
NP_000262.2:p.Val1212=
|
|