ENST00000240093.8:c.702T>G
MANE Select
|
ENSP00000240093.3:p.Pro234=
|
|
ENST00000240093.7:c.702T>G
|
ENSP00000240093.3:p.Pro234=
|
|
ENST00000537916.2:c.702T>G
|
ENSP00000437489.1:p.Pro234=
|
|
NM_017412.3:c.702T>G
|
NP_059108.1:p.Pro234=
|
|
NM_145866.1:c.702T>G
|
NP_665873.1:p.Pro234=
|
|
XM_011544646.1:c.585T>G
|
XP_011542948.1:p.Pro195=
|
|
XM_011544647.1:c.501T>G
|
XP_011542949.1:p.Pro167=
|
|
XM_011544648.1:c.702T>G
|
XP_011542950.1:p.Pro234=
|
|
XM_011544649.1:c.501T>G
|
XP_011542951.1:p.Pro167=
|
|
XR_949476.1:n.1221T>G
|
|
|
XR_949477.1:n.1221T>G
|
|
|
XR_949478.1:n.1221T>G
|
|
|
XM_017013841.1:c.501T>G
|
XP_016869330.1:p.Pro167=
|
|
XM_017013842.1:c.702T>G
|
XP_016869331.1:p.Pro234=
|
|
XM_017013843.1:c.702T>G
|
XP_016869332.1:p.Pro234=
|
|
XM_017013844.1:c.702T>G
|
XP_016869333.1:p.Pro234=
|
|
XR_001745597.2:n.1178T>G
|
|
|
XR_949476.2:n.1221T>G
|
|
|
NM_017412.4:c.702T>G
MANE Select
|
NP_059108.1:p.Pro234=
|
|
NM_145866.2:c.702T>G
|
NP_665873.1:p.Pro234=
|
|