|
NM_001199138.2:c.2631G>A
MANE Select
|
NP_001186067.1:p.Val877=
|
|
ENST00000402280.6:c.2631G>A
MANE Select
|
ENSP00000385428.1:p.Val877=
|
|
NM_001199138.1:c.2631G>A
|
NP_001186067.1:p.Val877=
|
|
NM_001199139.1:c.2631G>A
|
NP_001186068.1:p.Val877=
|
|
NM_001302504.1:c.636G>A
|
NP_001289433.1:p.Val212=
|
|
NM_021209.4:c.2631G>A
|
NP_067032.3:p.Val877=
|
|
ENST00000342905.10:c.636G>A
|
ENSP00000339666.6:p.Val212=
|
|
ENST00000360906.9:c.2631G>A
|
ENSP00000354159.5:p.Val877=
|
|
ENST00000402280.5:c.2631G>A
|
ENSP00000385428.1:p.Val877=
|
|
ENST00000404025.2:c.2631G>A
|
ENSP00000385090.2:p.Val877=
|
|
ENST00000404025.3:c.*337G>A
|
ENSP00000385090.3:n.*337G>A
|
|
ENST00000652197.1:c.*361G>A
|
ENSP00000498301.1:n.*361G>A
|
|
ENST00000652197.2:c.324G>A
|
ENSP00000498301.2:p.Val108=
|
|
XR_001738872.1:n.2897G>A
|
|