|
NM_080597.4:c.2624G>A
MANE Select
|
NP_542164.2:p.Arg875Gln
|
|
ENST00000319481.8:c.2624G>A
MANE Select
|
ENSP00000320291.3:p.Arg875Gln
|
|
NM_001242508.1:c.1478G>A
|
NP_001229437.1:p.Arg493Gln
|
|
NM_018030.4:c.1085G>A
|
NP_060500.3:p.Arg362Gln
|
|
NM_080597.3:c.2624G>A
|
NP_542164.2:p.Arg875Gln
|
|
ENST00000319481.7:c.2624G>A
|
ENSP00000320291.3:p.Arg875Gln
|
|
ENST00000357041.8:c.1478G>A
|
ENSP00000349545.4:p.Arg493Gln
|
|
ENST00000399443.7:c.1085G>A
|
ENSP00000382372.3:p.Arg362Gln
|
|
ENST00000578013.1:c.629G>A
|
ENSP00000464617.1:p.Arg210Gln
|
|
XM_006722380.2:c.2549G>A
|
XP_006722443.1:p.Arg850Gln
|
|
XM_006722380.3:c.2549G>A
|
XP_006722443.1:p.Arg850Gln
|
|
XM_006722381.2:c.2516G>A
|
XP_006722444.1:p.Arg839Gln
|
|
XM_006722382.2:c.2489G>A
|
XP_006722445.1:p.Arg830Gln
|
|
XM_006722382.4:c.2489G>A
|
XP_006722445.1:p.Arg830Gln
|
|
XM_006722383.2:c.2441G>A
|
XP_006722446.1:p.Arg814Gln
|
|
XM_017025530.1:c.2678G>A
|
XP_016881019.1:p.Arg893Gln
|
|
XM_017025531.2:c.2441G>A
|
XP_016881020.1:p.Arg814Gln
|
|
XM_017025533.2:c.1085G>A
|
XP_016881022.1:p.Arg362Gln
|
|
XR_001753139.2:n.2550G>A
|
|