ENST00000318158.11:c.897C>T
MANE Select
|
ENSP00000313432.6:p.His299=
|
|
ENST00000318158.10:c.897C>T
|
ENSP00000313432.6:p.His299=
|
|
ENST00000460882.5:n.924C>T
|
|
|
ENST00000480596.5:n.1598C>T
|
|
|
ENST00000491488.5:n.602C>T
|
|
|
ENST00000494290.1:c.*52-189C>T
|
ENSP00000432021.1:n.*52-189C>T
|
|
ENST00000497693.1:n.4465C>T
|
|
|
NM_012203.1:c.897C>T
|
NP_036335.1:p.His299=
|
|
XM_005251631.1:c.576C>T
|
XP_005251688.1:p.His192=
|
|
XM_011518073.1:c.495C>T
|
XP_011516375.1:p.His165=
|
|
XM_017015320.2:c.946-719C>T
|
XP_016870809.1:n.946-719C>T
|
|
XM_017015321.2:c.866-719C>T
|
XP_016870810.1:n.866-719C>T
|
|
XM_017015323.2:c.544-719C>T
|
XP_016870812.1:n.544-719C>T
|
|
XM_024447716.1:c.1219-719C>T
|
XP_024303484.1:n.1219-719C>T
|
|
XM_024447717.1:c.1139-719C>T
|
XP_024303485.1:n.1139-719C>T
|
|
XR_002956828.1:n.1234-719C>T
|
|
|
XR_002956829.1:n.1154-719C>T
|
|
|
XR_002956830.1:n.2317C>T
|
|
|
XR_002956831.1:n.1992C>T
|
|
|
XR_002956832.1:n.1316C>T
|
|
|
NM_012203.2:c.897C>T
MANE Select
|
NP_036335.1:p.His299=
|
|