ENST00000539111.7:c.562+18A>C
(POLG2)
MANE Select
|
ENSP00000442563.2:n.562+18A>C
|
|
ENST00000585104.2:n.533+18A>C
(POLG2)
|
|
|
ENST00000671755.1:c.533+18A>C
(POLG2)
|
|
|
ENST00000673460.1:c.533+18A>C
(POLG2)
|
|
|
ENST00000539111.6:c.562+18A>C
(POLG2)
|
ENSP00000442563.2:n.562+18A>C
|
|
ENST00000578997.1:c.224+143A>C
(POLG2)
|
ENSP00000464389.1:n.224+143A>C
|
|
ENST00000585141.5:n.613+18A>C
(POLG2)
|
|
|
NM_007215.3:c.562+18A>C
(POLG2)
|
NP_009146.2:n.562+18A>C
|
|
XM_006721651.2:c.562+18A>C
(POLG2)
|
XP_006721714.1:n.562+18A>C
|
|
XR_243630.1:n.613+18A>C
(POLG2)
|
|
|
XR_934357.1:n.613+18A>C
(POLG2)
|
|
|
XR_934358.1:n.613+18A>C
(POLG2)
|
|
|
XM_024450708.1:c.*97T>G
(MILR1)
|
XP_024306476.1:n.*97T>G
|
|
XR_002957990.1:n.1339T>G
(MILR1)
|
|
|
NM_007215.4:c.562+18A>C
(POLG2)
MANE Select
|
NP_009146.2:n.562+18A>C
|
|