ENST00000342494.8:c.2293T>G
MANE Select
|
ENSP00000340596.3:p.Ser765Ala
|
|
ENST00000342494.7:c.2293T>G
|
ENSP00000340596.3:p.Ser765Ala
|
|
ENST00000434735.6:c.2293T>G
|
ENSP00000391529.2:p.Ser765Ala
|
|
ENST00000449510.6:c.*263T>G
|
ENSP00000395802.2:n.*263T>G
|
|
ENST00000538070.1:n.1809T>G
|
|
|
ENST00000539584.5:n.1817T>G
|
|
|
ENST00000539599.5:c.2293T>G
|
ENSP00000443131.1:p.Ser765Ala
|
|
NM_130466.3:c.2293T>G
|
NP_569733.2:p.Ser765Ala
|
|
NM_183415.2:c.2293T>G
|
NP_904324.1:p.Ser765Ala
|
|
XM_005253987.1:c.2293T>G
|
XP_005254044.1:p.Ser765Ala
|
|
XM_006719681.2:c.2293T>G
|
XP_006719744.1:p.Ser765Ala
|
|
XM_006719682.1:c.2293T>G
|
XP_006719745.1:p.Ser765Ala
|
|
XM_011538959.1:c.2293T>G
|
XP_011537261.1:p.Ser765Ala
|
|
XM_011538960.1:c.2293T>G
|
XP_011537262.1:p.Ser765Ala
|
|
XM_011538961.1:c.2293T>G
|
XP_011537263.1:p.Ser765Ala
|
|
XM_011538962.1:c.2293T>G
|
XP_011537264.1:p.Ser765Ala
|
|
XR_429118.2:n.3120T>G
|
|
|
XM_005253987.2:c.2293T>G
|
XP_005254044.1:p.Ser765Ala
|
|
XM_006719681.3:c.2293T>G
|
XP_006719744.1:p.Ser765Ala
|
|
XM_006719682.2:c.2293T>G
|
XP_006719745.1:p.Ser765Ala
|
|
XM_011538959.2:c.2293T>G
|
XP_011537261.1:p.Ser765Ala
|
|
XM_017020195.1:c.1714T>G
|
XP_016875684.1:p.Ser572Ala
|
|
XM_024449269.1:c.1714T>G
|
XP_024305037.1:p.Ser572Ala
|
|
XR_429118.3:n.3120T>G
|
|
|
XR_429119.4:n.3309T>G
|
|
|
NM_130466.4:c.2293T>G
MANE Select
|
NP_569733.2:p.Ser765Ala
|
|
NM_183415.3:c.2293T>G
|
NP_904324.1:p.Ser765Ala
|
|