ENST00000242317.9:c.1603A=
MANE Select
|
ENSP00000242317.4:p.Thr535=
|
|
ENST00000242317.8:c.1603A=
|
ENSP00000242317.4:p.Thr535=
|
|
ENST00000442556.1:c.114A=
|
|
|
ENST00000470169.5:c.507-213A=
|
|
|
ENST00000485580.1:n.82A=
|
|
|
ENST00000614641.4:c.1615A=
|
ENSP00000480538.1:p.Thr539=
|
|
NM_001281428.1:c.1615A=
|
NP_001268357.1:p.Thr539=
|
|
NM_012144.3:c.1603A=
|
NP_036276.1:p.Thr535=
|
|
XM_006716758.2:c.1072A=
|
XP_006716821.1:p.Thr358=
|
|
XM_011517846.1:c.1615A=
|
XP_011516148.1:p.Thr539=
|
|
XM_011517847.1:c.1615A=
|
XP_011516149.1:p.Thr539=
|
|
XM_011517848.1:c.1357A=
|
XP_011516150.1:p.Thr453=
|
|
XM_011517849.1:c.1582-77A=
|
XP_011516151.1:n.1582-77A=
|
|
XR_929232.1:n.1836-77A=
|
|
|
XR_929233.1:n.1836-77A=
|
|
|
XR_929235.1:n.1578-77A=
|
|
|
XM_006716758.3:c.1072A=
|
XP_006716821.1:p.Thr358=
|
|
XM_011517846.2:c.1615A=
|
XP_011516148.1:p.Thr539=
|
|
XM_011517847.3:c.1615A=
|
XP_011516149.1:p.Thr539=
|
|
XM_011517848.2:c.1357A=
|
XP_011516150.1:p.Thr453=
|
|
XM_011517849.2:c.1582-77A=
|
XP_011516151.1:n.1582-77A=
|
|
XM_017014625.2:c.1345A=
|
XP_016870114.1:p.Thr449=
|
|
XR_002956774.1:n.1783-77A=
|
|
|
XR_929232.2:n.1783-77A=
|
|
|
XR_929233.2:n.1783-77A=
|
|
|
NM_012144.4:c.1603A=
MANE Select
|
NP_036276.1:p.Thr535=
|
|
NM_001281428.2:c.1615A=
|
NP_001268357.1:p.Thr539=
|
|