ENST00000318158.11:c.865+119A>T
MANE Select
|
ENSP00000313432.6:n.865+119A>T
|
|
ENST00000318158.10:c.865+119A>T
|
ENSP00000313432.6:n.865+119A>T
|
|
ENST00000460882.5:n.892+119A>T
|
|
|
ENST00000480596.5:n.1566+119A>T
|
|
|
ENST00000482603.1:n.318+119A>T
|
|
|
ENST00000491488.5:n.570+119A>T
|
|
|
ENST00000494290.1:c.*51+1106A>T
|
ENSP00000432021.1:n.*51+1106A>T
|
|
ENST00000497693.1:n.4433+119A>T
|
|
|
ENST00000512404.2:n.171A>T
|
|
|
ENST00000607784.1:c.865+119A>T
|
ENSP00000475569.1:n.865+119A>T
|
|
NM_012203.1:c.865+119A>T
|
NP_036335.1:n.865+119A>T
|
|
XM_005251631.1:c.544+119A>T
|
XP_005251688.1:n.544+119A>T
|
|
XM_011518073.1:c.463+119A>T
|
XP_011516375.1:n.463+119A>T
|
|
XM_017015320.2:c.865+119A>T
|
XP_016870809.1:n.865+119A>T
|
|
XM_017015321.2:c.865+119A>T
|
XP_016870810.1:n.865+119A>T
|
|
XM_017015323.2:c.463+119A>T
|
XP_016870812.1:n.463+119A>T
|
|
XM_024447716.1:c.1138+119A>T
|
XP_024303484.1:n.1138+119A>T
|
|
XM_024447717.1:c.1138+119A>T
|
XP_024303485.1:n.1138+119A>T
|
|
XR_002956828.1:n.1153+119A>T
|
|
|
XR_002956829.1:n.1153+119A>T
|
|
|
XR_002956830.1:n.2285+119A>T
|
|
|
XR_002956831.1:n.1960+119A>T
|
|
|
XR_002956832.1:n.1284+119A>T
|
|
|
NM_012203.2:c.865+119A>T
MANE Select
|
NP_036335.1:n.865+119A>T
|
|