ENST00000373247.7:c.*125G>T
MANE Select
|
ENSP00000362344.2:n.*125G>T
|
|
ENST00000373225.7:c.*125G>T
|
ENSP00000362322.3:n.*125G>T
|
|
ENST00000373247.6:c.*125G>T
|
ENSP00000362344.2:n.*125G>T
|
|
ENST00000393706.6:c.*125G>T
|
ENSP00000377309.2:n.*125G>T
|
|
ENST00000460181.5:n.1877G>T
|
|
|
ENST00000467826.5:n.709+406G>T
|
|
|
ENST00000630236.2:c.*613G>T
|
ENSP00000486766.1:n.*613G>T
|
|
NM_001018078.2:c.*125G>T
|
NP_001018088.1:n.*125G>T
|
|
NM_001288803.1:c.*125G>T
|
NP_001275732.1:n.*125G>T
|
|
NM_004957.5:c.*125G>T
|
NP_004948.4:n.*125G>T
|
|
NR_110170.1:n.1937G>T
|
|
|
XM_005251864.2:c.1483+406G>T
|
XP_005251921.1:n.1483+406G>T
|
|
XM_011518437.1:c.*125G>T
|
XP_011516739.1:n.*125G>T
|
|
XM_011518438.1:c.*125G>T
|
XP_011516740.1:n.*125G>T
|
|
XM_011518439.1:c.*125G>T
|
XP_011516741.1:n.*125G>T
|
|
XR_242581.2:n.1786G>T
|
|
|
XR_242582.2:n.1380+406G>T
|
|
|
XM_005251864.4:c.1483+406G>T
|
XP_005251921.1:n.1483+406G>T
|
|
XM_011518439.2:c.*125G>T
|
XP_011516741.1:n.*125G>T
|
|
XM_017014565.2:c.1333+406G>T
|
XP_016870054.1:n.1333+406G>T
|
|
XM_017014566.1:c.*125G>T
|
XP_016870055.1:n.*125G>T
|
|
XR_242581.4:n.1784G>T
|
|
|
XR_242582.4:n.1378+406G>T
|
|
|
NM_004957.6:c.*125G>T
MANE Select
|
NP_004948.4:n.*125G>T
|
|