ENST00000318158.11:c.946G>T
MANE Select
|
ENSP00000313432.6:p.Gly316Cys
|
|
ENST00000318158.10:c.946G>T
|
ENSP00000313432.6:p.Gly316Cys
|
|
ENST00000460882.5:n.973G>T
|
|
|
ENST00000480596.5:n.1647G>T
|
|
|
ENST00000494290.1:c.*52-140G>T
|
ENSP00000432021.1:n.*52-140G>T
|
|
ENST00000497693.1:n.4514G>T
|
|
|
NM_012203.1:c.946G>T
|
NP_036335.1:p.Gly316Cys
|
|
XM_005251631.1:c.625G>T
|
XP_005251688.1:p.Gly209Cys
|
|
XM_011518073.1:c.544G>T
|
XP_011516375.1:p.Gly182Cys
|
|
XM_017015320.2:c.946-670G>T
|
XP_016870809.1:n.946-670G>T
|
|
XM_017015321.2:c.866-670G>T
|
XP_016870810.1:n.866-670G>T
|
|
XM_017015323.2:c.544-670G>T
|
XP_016870812.1:n.544-670G>T
|
|
XM_024447716.1:c.1219-670G>T
|
XP_024303484.1:n.1219-670G>T
|
|
XM_024447717.1:c.1139-670G>T
|
XP_024303485.1:n.1139-670G>T
|
|
XR_002956828.1:n.1234-670G>T
|
|
|
XR_002956829.1:n.1154-670G>T
|
|
|
XR_002956830.1:n.2366G>T
|
|
|
XR_002956831.1:n.2041G>T
|
|
|
XR_002956832.1:n.1365G>T
|
|
|
NM_012203.2:c.946G>T
MANE Select
|
NP_036335.1:p.Gly316Cys
|
|