ENST00000318158.11:c.899G>T
MANE Select
|
ENSP00000313432.6:p.Arg300Ile
|
|
ENST00000318158.10:c.899G>T
|
ENSP00000313432.6:p.Arg300Ile
|
|
ENST00000460882.5:n.926G>T
|
|
|
ENST00000480596.5:n.1600G>T
|
|
|
ENST00000494290.1:c.*52-187G>T
|
ENSP00000432021.1:n.*52-187G>T
|
|
ENST00000497693.1:n.4467G>T
|
|
|
NM_012203.1:c.899G>T
|
NP_036335.1:p.Arg300Ile
|
|
XM_005251631.1:c.578G>T
|
XP_005251688.1:p.Arg193Ile
|
|
XM_011518073.1:c.497G>T
|
XP_011516375.1:p.Arg166Ile
|
|
XM_017015320.2:c.946-717G>T
|
XP_016870809.1:n.946-717G>T
|
|
XM_017015321.2:c.866-717G>T
|
XP_016870810.1:n.866-717G>T
|
|
XM_017015323.2:c.544-717G>T
|
XP_016870812.1:n.544-717G>T
|
|
XM_024447716.1:c.1219-717G>T
|
XP_024303484.1:n.1219-717G>T
|
|
XM_024447717.1:c.1139-717G>T
|
XP_024303485.1:n.1139-717G>T
|
|
XR_002956828.1:n.1234-717G>T
|
|
|
XR_002956829.1:n.1154-717G>T
|
|
|
XR_002956830.1:n.2319G>T
|
|
|
XR_002956831.1:n.1994G>T
|
|
|
XR_002956832.1:n.1318G>T
|
|
|
NM_012203.2:c.899G>T
MANE Select
|
NP_036335.1:p.Arg300Ile
|
|