ENST00000317357.10:c.1847G>A
MANE Select
|
ENSP00000318900.5:p.Gly616Asp
|
|
ENST00000317357.9:c.1847G>A
|
ENSP00000318900.5:p.Gly616Asp
|
|
NM_018013.3:c.1847G>A
|
NP_060483.3:p.Gly616Asp
|
|
XM_005267041.3:c.2000G>A
|
XP_005267098.1:p.Gly667Asp
|
|
XM_005267042.3:c.1904G>A
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XP_005267099.1:p.Gly635Asp
|
|
XM_011535920.1:c.2000G>A
|
XP_011534222.1:p.Gly667Asp
|
|
XM_011535921.1:c.1886G>A
|
XP_011534223.1:p.Gly629Asp
|
|
XM_011535922.1:c.1259G>A
|
XP_011534224.1:p.Gly420Asp
|
|
XM_011535923.1:c.1070G>A
|
XP_011534225.1:p.Gly357Asp
|
|
XM_005267041.4:c.2000G>A
|
XP_005267098.1:p.Gly667Asp
|
|
XM_005267042.4:c.1904G>A
|
XP_005267099.1:p.Gly635Asp
|
|
XM_011535920.2:c.2000G>A
|
XP_011534222.1:p.Gly667Asp
|
|
XM_011535921.2:c.1886G>A
|
XP_011534223.1:p.Gly629Asp
|
|
XM_011535923.2:c.1070G>A
|
XP_011534225.1:p.Gly357Asp
|
|
XM_017010991.1:c.1400G>A
|
XP_016866480.1:p.Gly467Asp
|
|
XM_017010992.1:c.1400G>A
|
XP_016866481.1:p.Gly467Asp
|
|
XM_017010993.1:c.1400G>A
|
XP_016866482.1:p.Gly467Asp
|
|
XM_017010994.1:c.1400G>A
|
XP_016866483.1:p.Gly467Asp
|
|
NM_018013.4:c.1847G>A
MANE Select
|
NP_060483.3:p.Gly616Asp
|
|