ENST00000373247.7:c.1506G>T
MANE Select
|
ENSP00000362344.2:p.Leu502=
|
|
ENST00000373225.7:c.1356G>T
|
ENSP00000362322.3:p.Leu452=
|
|
ENST00000373228.5:c.*163G>T
|
ENSP00000362325.1:n.*163G>T
|
|
ENST00000373247.6:c.1506G>T
|
ENSP00000362344.2:p.Leu502=
|
|
ENST00000393706.6:c.1428G>T
|
ENSP00000377309.2:p.Leu476=
|
|
ENST00000460181.5:n.1494G>T
|
|
|
ENST00000467826.5:n.709+23G>T
|
|
|
ENST00000475270.1:n.332G>T
|
|
|
ENST00000630236.2:c.*230G>T
|
ENSP00000486766.1:n.*230G>T
|
|
NM_001018078.2:c.1356G>T
|
NP_001018088.1:p.Leu452=
|
|
NM_001288803.1:c.1428G>T
|
NP_001275732.1:p.Leu476=
|
|
NM_004957.5:c.1506G>T
|
NP_004948.4:p.Leu502=
|
|
NR_110170.1:n.1554G>T
|
|
|
XM_005251864.2:c.1483+23G>T
|
XP_005251921.1:n.1483+23G>T
|
|
XM_011518437.1:c.1356G>T
|
XP_011516739.1:p.Leu452=
|
|
XM_011518438.1:c.1356G>T
|
XP_011516740.1:p.Leu452=
|
|
XM_011518439.1:c.663G>T
|
XP_011516741.1:p.Leu221=
|
|
XR_242581.2:n.1403G>T
|
|
|
XR_242582.2:n.1380+23G>T
|
|
|
XM_005251864.4:c.1483+23G>T
|
XP_005251921.1:n.1483+23G>T
|
|
XM_011518439.2:c.663G>T
|
XP_011516741.1:p.Leu221=
|
|
XM_017014565.2:c.1333+23G>T
|
XP_016870054.1:n.1333+23G>T
|
|
XM_017014566.1:c.663G>T
|
XP_016870055.1:p.Leu221=
|
|
XR_242581.4:n.1401G>T
|
|
|
XR_242582.4:n.1378+23G>T
|
|
|
NM_004957.6:c.1506G>T
MANE Select
|
NP_004948.4:p.Leu502=
|
|