|
NM_014362.4:c.948G>C
MANE Select
|
NP_055177.2:p.Glu316Asp
|
|
ENST00000359678.10:c.948G>C
MANE Select
|
ENSP00000352706.5:p.Glu316Asp
|
|
NM_014362.3:c.948G>C
|
NP_055177.2:p.Glu316Asp
|
|
NM_198047.2:c.948G>C
|
NP_932164.1:p.Glu316Asp
|
|
NM_198047.3:c.948G>C
|
NP_932164.1:p.Glu316Asp
|
|
ENST00000359678.9:c.948G>C
|
ENSP00000352706.5:p.Glu316Asp
|
|
ENST00000392332.7:c.948G>C
|
ENSP00000376144.3:p.Glu316Asp
|
|
ENST00000409820.2:c.288G>C
|
ENSP00000387098.2:p.Glu96Asp
|
|
ENST00000410045.5:c.279G>C
|
ENSP00000386274.1:p.Glu93Asp
|
|
ENST00000416732.5:c.201G>C
|
ENSP00000399263.1:p.Glu67Asp
|
|
ENST00000486981.1:n.217G>C
|
|
|
ENST00000489147.1:n.3091G>C
|
|
|
ENST00000622246.4:c.930G>C
|
ENSP00000481055.1:p.Glu310Asp
|
|
XM_011510953.1:c.948G>C
|
XP_011509255.1:p.Glu316Asp
|
|
XM_011510953.2:c.948G>C
|
XP_011509255.1:p.Glu316Asp
|
|
XM_011510954.1:c.450G>C
|
XP_011509256.1:p.Glu150Asp
|
|
XR_922903.1:n.1192G>C
|
|
|
XR_922903.2:n.1011G>C
|
|