ENST00000317357.10:c.2041G>C
MANE Select
|
ENSP00000318900.5:p.Glu681Gln
|
|
ENST00000317357.9:c.2041G>C
|
ENSP00000318900.5:p.Glu681Gln
|
|
NM_018013.3:c.2041G>C
|
NP_060483.3:p.Glu681Gln
|
|
XM_005267041.3:c.2194G>C
|
XP_005267098.1:p.Glu732Gln
|
|
XM_005267042.3:c.2098G>C
|
XP_005267099.1:p.Glu700Gln
|
|
XM_011535920.1:c.2194G>C
|
XP_011534222.1:p.Glu732Gln
|
|
XM_011535921.1:c.2080G>C
|
XP_011534223.1:p.Glu694Gln
|
|
XM_011535922.1:c.1453G>C
|
XP_011534224.1:p.Glu485Gln
|
|
XM_011535923.1:c.1264G>C
|
XP_011534225.1:p.Glu422Gln
|
|
XM_005267041.4:c.2194G>C
|
XP_005267098.1:p.Glu732Gln
|
|
XM_005267042.4:c.2098G>C
|
XP_005267099.1:p.Glu700Gln
|
|
XM_011535920.2:c.2194G>C
|
XP_011534222.1:p.Glu732Gln
|
|
XM_011535921.2:c.2080G>C
|
XP_011534223.1:p.Glu694Gln
|
|
XM_011535923.2:c.1264G>C
|
XP_011534225.1:p.Glu422Gln
|
|
XM_017010991.1:c.1594G>C
|
XP_016866480.1:p.Glu532Gln
|
|
XM_017010992.1:c.1594G>C
|
XP_016866481.1:p.Glu532Gln
|
|
XM_017010993.1:c.1594G>C
|
XP_016866482.1:p.Glu532Gln
|
|
XM_017010994.1:c.1594G>C
|
XP_016866483.1:p.Glu532Gln
|
|
NM_018013.4:c.2041G>C
MANE Select
|
NP_060483.3:p.Glu681Gln
|
|