|
NM_001754.5:c.36G>T
MANE Select
|
NP_001745.2:p.Ser12=
|
|
ENST00000675419.1:c.36G>T
MANE Select
|
ENSP00000501943.1:p.Ser12=
|
|
NM_001754.4:c.36G>T , LRG_482t1:c.36G>T
|
NP_001745.2:p.Ser12=
|
|
ENST00000300305.7:c.36G>T
|
ENSP00000300305.3:p.Ser12=
|
|
ENST00000416754.1:c.36G>T
|
ENSP00000405158.1:p.Ser12=
|
|
ENST00000437180.5:c.36G>T
|
ENSP00000409227.1:p.Ser12=
|
|
ENST00000455571.5:c.36G>T
|
ENSP00000388189.1:p.Ser12=
|
|
ENST00000475045.6:c.36G>T
|
ENSP00000477072.1:p.Ser12=
|
|
ENST00000482318.5:c.36G>T
|
ENSP00000477067.1:p.Ser12=
|
|
XM_005261069.3:c.36G>T
|
XP_005261126.1:p.Ser12=
|
|
XM_005261069.4:c.36G>T
|
XP_005261126.1:p.Ser12=
|
|
XM_011529766.1:c.36G>T
|
XP_011528068.1:p.Ser12=
|
|
XM_011529766.2:c.36G>T
|
XP_011528068.1:p.Ser12=
|
|
XM_011529767.1:c.36G>T
|
XP_011528069.1:p.Ser12=
|
|
XM_011529767.2:c.36G>T
|
XP_011528069.1:p.Ser12=
|
|
XM_011529768.1:c.36G>T
|
XP_011528070.1:p.Ser12=
|
|
XM_011529768.2:c.36G>T
|
XP_011528070.1:p.Ser12=
|
|
XM_011529770.1:c.36G>T
|
XP_011528072.1:p.Ser12=
|
|
XM_011529770.2:c.36G>T
|
XP_011528072.1:p.Ser12=
|
|
XR_937576.1:n.215G>T
|
|
|
XR_937576.2:n.262G>T
|
|
