ENST00000373247.7:c.1761G>T
MANE Select
|
ENSP00000362344.2:p.Gln587His
|
|
ENST00000373225.7:c.1611G>T
|
ENSP00000362322.3:p.Gln537His
|
|
ENST00000373247.6:c.1761G>T
|
ENSP00000362344.2:p.Gln587His
|
|
ENST00000393706.6:c.1683G>T
|
ENSP00000377309.2:p.Gln561His
|
|
ENST00000460181.5:n.1749G>T
|
|
|
ENST00000467826.5:n.709+278G>T
|
|
|
ENST00000630236.2:c.*485G>T
|
ENSP00000486766.1:n.*485G>T
|
|
NM_001018078.2:c.1611G>T
|
NP_001018088.1:p.Gln537His
|
|
NM_001288803.1:c.1683G>T
|
NP_001275732.1:p.Gln561His
|
|
NM_004957.5:c.1761G>T
|
NP_004948.4:p.Gln587His
|
|
NR_110170.1:n.1809G>T
|
|
|
XM_005251864.2:c.1483+278G>T
|
XP_005251921.1:n.1483+278G>T
|
|
XM_011518437.1:c.1611G>T
|
XP_011516739.1:p.Gln537His
|
|
XM_011518438.1:c.1611G>T
|
XP_011516740.1:p.Gln537His
|
|
XM_011518439.1:c.918G>T
|
XP_011516741.1:p.Gln306His
|
|
XR_242581.2:n.1658G>T
|
|
|
XR_242582.2:n.1380+278G>T
|
|
|
XM_005251864.4:c.1483+278G>T
|
XP_005251921.1:n.1483+278G>T
|
|
XM_011518439.2:c.918G>T
|
XP_011516741.1:p.Gln306His
|
|
XM_017014565.2:c.1333+278G>T
|
XP_016870054.1:n.1333+278G>T
|
|
XM_017014566.1:c.918G>T
|
XP_016870055.1:p.Gln306His
|
|
XR_242581.4:n.1656G>T
|
|
|
XR_242582.4:n.1378+278G>T
|
|
|
NM_004957.6:c.1761G>T
MANE Select
|
NP_004948.4:p.Gln587His
|
|