ENST00000235521.5:c.827T>G
MANE Select
|
ENSP00000235521.4:p.Val276Gly
|
|
ENST00000235521.4:c.827T>G
|
ENSP00000235521.4:p.Val276Gly
|
|
ENST00000369426.9:c.*193T>G
|
ENSP00000358434.5:n.*193T>G
|
|
NM_015836.3:c.827T>G
|
NP_056651.1:p.Val276Gly
|
|
NM_201263.2:c.*193T>G
|
NP_957715.1:n.*193T>G
|
|
XM_005270350.2:c.773T>G
|
XP_005270407.1:p.Val258Gly
|
|
XM_006710283.1:c.545T>G
|
XP_006710346.1:p.Val182Gly
|
|
XM_011540493.1:c.758T>G
|
XP_011538795.1:p.Val253Gly
|
|
XM_011540494.1:c.758T>G
|
XP_011538796.1:p.Val253Gly
|
|
XM_011540495.1:c.569T>G
|
XP_011538797.1:p.Val190Gly
|
|
XM_005270350.3:c.773T>G
|
XP_005270407.1:p.Val258Gly
|
|
XM_011540494.2:c.758T>G
|
XP_011538796.1:p.Val253Gly
|
|
XM_011540495.2:c.569T>G
|
XP_011538797.1:p.Val190Gly
|
|
XM_017000038.1:c.770T>G
|
XP_016855527.1:p.Val257Gly
|
|
XM_017000039.1:c.758T>G
|
XP_016855528.1:p.Val253Gly
|
|
XM_017000040.1:c.656T>G
|
XP_016855529.1:p.Val219Gly
|
|
XM_017000041.2:c.488T>G
|
XP_016855530.1:p.Val163Gly
|
|
XM_017000042.1:c.*162T>G
|
XP_016855531.1:n.*162T>G
|
|
XM_024449826.1:c.758T>G
|
XP_024305594.1:p.Val253Gly
|
|
XM_024449860.1:c.545T>G
|
XP_024305628.1:p.Val182Gly
|
|
XM_024449871.1:c.545T>G
|
XP_024305639.1:p.Val182Gly
|
|
NM_001378226.1:c.758T>G
|
NP_001365155.1:p.Val253Gly
|
|
NM_001378227.1:c.758T>G
|
NP_001365156.1:p.Val253Gly
|
|
NM_001378228.1:c.656T>G
|
NP_001365157.1:p.Val219Gly
|
|
NM_001378229.1:c.569T>G
|
NP_001365158.1:p.Val190Gly
|
|
NM_001378230.1:c.545T>G
|
NP_001365159.1:p.Val182Gly
|
|
NM_001378231.1:c.*162T>G
|
NP_001365160.1:n.*162T>G
|
|
NM_015836.4:c.827T>G
MANE Select
|
NP_056651.1:p.Val276Gly
|
|