ENST00000318158.11:c.878A>G
MANE Select
|
ENSP00000313432.6:p.His293Arg
|
|
ENST00000318158.10:c.878A>G
|
ENSP00000313432.6:p.His293Arg
|
|
ENST00000460882.5:n.905A>G
|
|
|
ENST00000480596.5:n.1579A>G
|
|
|
ENST00000491488.5:n.583A>G
|
|
|
ENST00000494290.1:c.*52-208A>G
|
ENSP00000432021.1:n.*52-208A>G
|
|
ENST00000497693.1:n.4446A>G
|
|
|
NM_012203.1:c.878A>G
|
NP_036335.1:p.His293Arg
|
|
XM_005251631.1:c.557A>G
|
XP_005251688.1:p.His186Arg
|
|
XM_011518073.1:c.476A>G
|
XP_011516375.1:p.His159Arg
|
|
XM_017015320.2:c.946-738A>G
|
XP_016870809.1:n.946-738A>G
|
|
XM_017015321.2:c.866-738A>G
|
XP_016870810.1:n.866-738A>G
|
|
XM_017015323.2:c.544-738A>G
|
XP_016870812.1:n.544-738A>G
|
|
XM_024447716.1:c.1219-738A>G
|
XP_024303484.1:n.1219-738A>G
|
|
XM_024447717.1:c.1139-738A>G
|
XP_024303485.1:n.1139-738A>G
|
|
XR_002956828.1:n.1234-738A>G
|
|
|
XR_002956829.1:n.1154-738A>G
|
|
|
XR_002956830.1:n.2298A>G
|
|
|
XR_002956831.1:n.1973A>G
|
|
|
XR_002956832.1:n.1297A>G
|
|
|
NM_012203.2:c.878A>G
MANE Select
|
NP_036335.1:p.His293Arg
|
|