ENST00000325631.10:c.*193A>G
MANE Select
|
ENSP00000323264.5:n.*193A>G
|
|
ENST00000413223.3:c.*162+31A>G
|
ENSP00000398922.2:n.*162+31A>G
|
|
ENST00000436532.7:c.1522A>G
|
ENSP00000414776.2:n.1522A>G
|
|
ENST00000645446.1:c.*193A>G
|
ENSP00000494616.1:n.*193A>G
|
|
ENST00000647531.1:c.*193A>G
|
ENSP00000493858.1:n.*193A>G
|
|
ENST00000325631.9:c.*193A>G
|
ENSP00000323264.5:n.*193A>G
|
|
ENST00000413223.2:c.*162+31A>G
|
ENSP00000398922.2:n.*162+31A>G
|
|
ENST00000436532.6:c.*193A>G
|
ENSP00000414776.2:n.*193A>G
|
|
ENST00000454295.6:c.*193A>G
|
ENSP00000396244.2:n.*193A>G
|
|
NM_001038603.2:c.*193A>G
|
NP_001033692.2:n.*193A>G
|
|
NM_001244734.1:c.*193A>G
|
NP_001231663.1:n.*193A>G
|
|
XM_005248445.3:c.*193A>G
|
XP_005248502.1:n.*193A>G
|
|
XM_005248446.3:c.*193A>G
|
XP_005248503.1:n.*193A>G
|
|
XM_005248447.3:c.*193A>G
|
XP_005248504.1:n.*193A>G
|
|
XM_005248445.4:c.*193A>G
|
XP_005248502.1:n.*193A>G
|
|
XM_005248446.4:c.*193A>G
|
XP_005248503.1:n.*193A>G
|
|
XM_005248447.4:c.*193A>G
|
XP_005248504.1:n.*193A>G
|
|
NM_001038603.3:c.*193A>G
MANE Select
|
NP_001033692.2:n.*193A>G
|
|
NM_001244734.2:c.*193A>G
|
NP_001231663.1:n.*193A>G
|
|