ENST00000539111.7:c.556C>T
(POLG2)
MANE Select
|
ENSP00000442563.2:p.Leu186Phe
|
|
ENST00000585104.2:n.527C>T
(POLG2)
|
|
|
ENST00000671755.1:c.527C>T
(POLG2)
|
|
|
ENST00000673460.1:c.527C>T
(POLG2)
|
|
|
ENST00000539111.6:c.556C>T
(POLG2)
|
ENSP00000442563.2:p.Leu186Phe
|
|
ENST00000578997.1:c.224+119C>T
(POLG2)
|
ENSP00000464389.1:n.224+119C>T
|
|
ENST00000585141.5:n.607C>T
(POLG2)
|
|
|
NM_007215.3:c.556C>T
(POLG2)
|
NP_009146.2:p.Leu186Phe
|
|
XM_006721651.2:c.556C>T
(POLG2)
|
XP_006721714.1:p.Leu186Phe
|
|
XR_243630.1:n.607C>T
(POLG2)
|
|
|
XR_934357.1:n.607C>T
(POLG2)
|
|
|
XR_934358.1:n.607C>T
(POLG2)
|
|
|
XM_024450708.1:c.*121G>A
(MILR1)
|
XP_024306476.1:n.*121G>A
|
|
XR_002957990.1:n.1363G>A
(MILR1)
|
|
|
NM_007215.4:c.556C>T
(POLG2)
MANE Select
|
NP_009146.2:p.Leu186Phe
|
|