ENST00000369244.7:c.1638G>C
MANE Select
|
ENSP00000358247.1:p.Val546=
|
|
ENST00000229971.2:c.1638G>C
|
ENSP00000229971.1:p.Val546=
|
|
ENST00000369244.6:c.1638G>C
|
ENSP00000358247.1:p.Val546=
|
|
NM_001278716.1:c.1638G>C
|
NP_001265645.1:p.Val546=
|
|
NM_012160.4:c.1638G>C
|
NP_036292.2:p.Val546=
|
|
NR_103836.1:n.1683G>C
|
|
|
XM_005266930.1:c.1566G>C
|
XP_005266987.1:p.Val522=
|
|
XM_005266930.3:c.1566G>C
|
XP_005266987.1:p.Val522=
|
|
XM_017010726.1:c.1638G>C
|
XP_016866215.1:p.Val546=
|
|
XM_017010727.2:c.1566G>C
|
XP_016866216.1:p.Val522=
|
|
XM_017010728.1:c.912G>C
|
XP_016866217.1:p.Val304=
|
|
NM_001278716.2:c.1638G>C
MANE Select
|
NP_001265645.1:p.Val546=
|
|
NR_103836.2:n.1623G>C
|
|
|
NM_012160.5:c.1638G>C
|
NP_036292.2:p.Val546=
|
|