|
NM_007215.4:c.775C>T
(POLG2)
MANE Select
|
NP_009146.2:p.Arg259Ter
|
|
ENST00000539111.7:c.775C>T
(POLG2)
MANE Select
|
ENSP00000442563.2:p.Arg259Ter
|
|
NM_007215.3:c.775C>T
(POLG2)
|
NP_009146.2:p.Arg259Ter
|
|
ENST00000539111.6:c.775C>T
(POLG2)
|
ENSP00000442563.2:p.Arg259Ter
|
|
ENST00000578687.5:n.102C>T
(POLG2)
|
|
|
ENST00000578997.1:c.437C>T
(POLG2)
|
ENSP00000464389.1:n.437C>T
|
|
ENST00000580893.5:n.213C>T
(POLG2)
|
|
|
ENST00000581355.1:c.34C>T
(POLG2)
|
ENSP00000462071.1:p.Arg12Ter
|
|
ENST00000585104.2:n.746C>T
(POLG2)
|
|
|
ENST00000585141.5:n.826C>T
(POLG2)
|
|
|
ENST00000671755.1:c.746C>T
(POLG2)
|
|
|
ENST00000673460.1:c.746C>T
(POLG2)
|
|
|
XM_006721651.2:c.775C>T
(POLG2)
|
XP_006721714.1:p.Arg259Ter
|
|
XM_024450706.1:c.*431G>A
(MILR1)
|
XP_024306474.1:n.*431G>A
|
|
XM_024450708.1:c.*29-3634G>A
(MILR1)
|
XP_024306476.1:n.*29-3634G>A
|
|
XR_002957989.1:n.1270+340G>A
(MILR1)
|
|
|
XR_002957990.1:n.1270+340G>A
(MILR1)
|
|
|
XR_243630.1:n.826C>T
(POLG2)
|
|
|
XR_934357.1:n.826C>T
(POLG2)
|
|
|
XR_934358.1:n.826C>T
(POLG2)
|
|