ENST00000539111.7:c.1105A>G
(POLG2)
MANE Select
|
ENSP00000442563.2:p.Arg369Gly
|
|
ENST00000585104.2:n.1076A>G
(POLG2)
|
|
|
ENST00000671755.1:c.1076A>G
(POLG2)
|
|
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ENST00000673460.1:c.1342A>G
(POLG2)
|
|
|
ENST00000539111.6:c.1105A>G
(POLG2)
|
ENSP00000442563.2:p.Arg369Gly
|
|
ENST00000577506.5:n.310A>G
(POLG2)
|
|
|
ENST00000581355.1:c.364A>G
(POLG2)
|
ENSP00000462071.1:p.Arg122Gly
|
|
ENST00000582501.5:n.713A>G
(POLG2)
|
|
|
ENST00000585104.1:n.62A>G
(POLG2)
|
|
|
ENST00000585141.5:n.1156A>G
(POLG2)
|
|
|
NM_007215.3:c.1105A>G
(POLG2)
|
NP_009146.2:p.Arg369Gly
|
|
XR_243630.1:n.1156A>G
(POLG2)
|
|
|
XR_934357.1:n.1156A>G
(POLG2)
|
|
|
XR_934358.1:n.1156A>G
(POLG2)
|
|
|
XM_024450706.1:c.*29-6552T>C
(MILR1)
|
XP_024306474.1:n.*29-6552T>C
|
|
XM_024450708.1:c.*29-10588T>C
(MILR1)
|
XP_024306476.1:n.*29-10588T>C
|
|
XR_002957989.1:n.1208-6552T>C
(MILR1)
|
|
|
XR_002957990.1:n.1208-6552T>C
(MILR1)
|
|
|
NM_007215.4:c.1105A>G
(POLG2)
MANE Select
|
NP_009146.2:p.Arg369Gly
|
|