|
ENST00000251127.11:c.800G>C
MANE Select
|
ENSP00000251127.6:p.Gly267Ala
|
|
|
ENST00000648359.1:c.800G>C
|
ENSP00000497465.1:p.Gly267Ala
|
|
|
ENST00000674840.1:n.898G>C
|
|
|
|
ENST00000674904.1:n.880G>C
|
|
|
|
ENST00000675075.1:n.402G>C
|
|
|
|
ENST00000675150.1:c.800G>C
|
ENSP00000502680.1:p.Gly267Ala
|
|
|
ENST00000675332.1:c.800G>C
|
ENSP00000501955.1:p.Gly267Ala
|
|
|
ENST00000675415.1:n.983G>C
|
|
|
|
ENST00000675594.1:c.*237G>C
|
ENSP00000502490.1:n.*237G>C
|
|
|
ENST00000675802.1:c.800G>C
|
ENSP00000501818.1:p.Gly267Ala
|
|
|
ENST00000676315.1:c.800G>C
|
ENSP00000501603.1:p.Gly267Ala
|
|
|
ENST00000676439.1:n.974G>C
|
|
|
|
ENST00000251127.10:c.800G>C
|
ENSP00000251127.6:p.Gly267Ala
|
|
|
ENST00000470333.1:n.896G>C
|
|
|
|
ENST00000497170.5:n.954G>C
|
|
|
|
NM_052867.2:c.800G>C
|
NP_443099.1:p.Gly267Ala
|
|
|
XM_011521067.1:c.857G>C
|
XP_011519369.1:p.Gly286Ala
|
|
|
XM_011521068.1:c.800G>C
|
XP_011519370.1:p.Gly267Ala
|
|
|
XM_011521069.1:c.857G>C
|
XP_011519371.1:p.Gly286Ala
|
|
|
XM_011521070.1:c.857G>C
|
XP_011519372.1:p.Gly286Ala
|
|
|
NM_001350748.1:c.800G>C
|
NP_001337677.1:p.Gly267Ala
|
|
|
NM_001350749.1:c.800G>C
|
NP_001337678.1:p.Gly267Ala
|
|
|
NM_001350750.1:c.800G>C
|
NP_001337679.1:p.Gly267Ala
|
|
|
NM_001350751.1:c.800G>C
|
NP_001337680.1:p.Gly267Ala
|
|
|
NM_052867.3:c.800G>C
|
NP_443099.1:p.Gly267Ala
|
|
|
XM_011521067.2:c.857G>C
|
XP_011519369.1:p.Gly286Ala
|
|
|
XM_011521069.2:c.857G>C
|
XP_011519371.1:p.Gly286Ala
|
|
|
XM_017020536.2:c.353G>C
|
XP_016876025.1:p.Gly118Ala
|
|
|
XM_017020537.1:c.35G>C
|
XP_016876026.1:p.Arg12Thr
|
|
|
XM_024449336.1:c.857G>C
|
XP_024305104.1:p.Gly286Ala
|
|
|
NM_052867.4:c.800G>C
MANE Select
|
NP_443099.1:p.Gly267Ala
|
|
|
NM_001350748.2:c.800G>C
|
NP_001337677.1:p.Gly267Ala
|
|
|
NM_001350749.2:c.800G>C
|
NP_001337678.1:p.Gly267Ala
|
|
|
NM_001350750.2:c.800G>C
|
NP_001337679.1:p.Gly267Ala
|
|
|
NM_001350751.2:c.800G>C
|
NP_001337680.1:p.Gly267Ala
|
|
