ENST00000318158.11:c.794C>T
MANE Select
|
ENSP00000313432.6:p.Ala265Val
|
|
ENST00000318158.10:c.794C>T
|
ENSP00000313432.6:p.Ala265Val
|
|
ENST00000460882.5:n.821C>T
|
|
|
ENST00000480596.5:n.1495C>T
|
|
|
ENST00000482603.1:n.247C>T
|
|
|
ENST00000491488.5:n.499C>T
|
|
|
ENST00000494290.1:c.*51+916C>T
|
ENSP00000432021.1:n.*51+916C>T
|
|
ENST00000497693.1:n.4362C>T
|
|
|
ENST00000607784.1:c.794C>T
|
ENSP00000475569.1:p.Ala265Val
|
|
NM_012203.1:c.794C>T
|
NP_036335.1:p.Ala265Val
|
|
XM_005251631.1:c.473C>T
|
XP_005251688.1:p.Ala158Val
|
|
XM_011518073.1:c.392C>T
|
XP_011516375.1:p.Ala131Val
|
|
XM_017015320.2:c.794C>T
|
XP_016870809.1:p.Ala265Val
|
|
XM_017015321.2:c.794C>T
|
XP_016870810.1:p.Ala265Val
|
|
XM_017015323.2:c.392C>T
|
XP_016870812.1:p.Ala131Val
|
|
XM_024447716.1:c.1067C>T
|
XP_024303484.1:p.Ala356Val
|
|
XM_024447717.1:c.1067C>T
|
XP_024303485.1:p.Ala356Val
|
|
XR_002956828.1:n.1082C>T
|
|
|
XR_002956829.1:n.1082C>T
|
|
|
XR_002956830.1:n.2214C>T
|
|
|
XR_002956831.1:n.1889C>T
|
|
|
XR_002956832.1:n.1213C>T
|
|
|
NM_012203.2:c.794C>T
MANE Select
|
NP_036335.1:p.Ala265Val
|
|