ENST00000487099.7:c.143-10914T>A
MANE Select
|
ENSP00000420267.1:n.143-10914T>A
|
|
ENST00000344523.8:c.143-10914T>A
|
ENSP00000341135.4:n.143-10914T>A
|
|
ENST00000373584.7:c.143-10926T>A
|
ENSP00000362686.3:n.143-10926T>A
|
|
ENST00000416460.6:c.143-10926T>A
|
ENSP00000413701.2:n.143-10926T>A
|
|
ENST00000475178.1:c.17-10914T>A
|
ENSP00000420587.1:n.17-10914T>A
|
|
ENST00000487099.6:c.143-10914T>A
|
ENSP00000420267.1:n.143-10914T>A
|
|
NM_001278546.1:c.143-10926T>A
|
NP_001265475.1:n.143-10926T>A
|
|
NM_001489.4:c.143-10926T>A
|
NP_001480.3:n.143-10926T>A
|
|
NM_033334.3:c.143-10914T>A
|
NP_201591.2:n.143-10914T>A
|
|
XM_005251917.3:c.143-10914T>A
|
XP_005251974.1:n.143-10914T>A
|
|
XM_005251918.3:c.17-10914T>A
|
XP_005251975.1:n.17-10914T>A
|
|
XM_005251917.5:c.143-10914T>A
|
XP_005251974.1:n.143-10914T>A
|
|
XM_005251918.5:c.17-10914T>A
|
XP_005251975.1:n.17-10914T>A
|
|
NM_033334.4:c.143-10914T>A
MANE Select
|
NP_201591.2:n.143-10914T>A
|
|
NM_001278546.2:c.143-10926T>A
|
NP_001265475.1:n.143-10926T>A
|
|
NM_001489.5:c.143-10926T>A
|
NP_001480.3:n.143-10926T>A
|
|