ENST00000317357.10:c.1736G>T
MANE Select
|
ENSP00000318900.5:p.Gly579Val
|
|
ENST00000317357.9:c.1736G>T
|
ENSP00000318900.5:p.Gly579Val
|
|
NM_018013.3:c.1736G>T
|
NP_060483.3:p.Gly579Val
|
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XM_005267041.3:c.1889G>T
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XP_005267098.1:p.Gly630Val
|
|
XM_005267042.3:c.1793G>T
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XP_005267099.1:p.Gly598Val
|
|
XM_011535920.1:c.1889G>T
|
XP_011534222.1:p.Gly630Val
|
|
XM_011535921.1:c.1775G>T
|
XP_011534223.1:p.Gly592Val
|
|
XM_011535922.1:c.1148G>T
|
XP_011534224.1:p.Gly383Val
|
|
XM_011535923.1:c.959G>T
|
XP_011534225.1:p.Gly320Val
|
|
XM_005267041.4:c.1889G>T
|
XP_005267098.1:p.Gly630Val
|
|
XM_005267042.4:c.1793G>T
|
XP_005267099.1:p.Gly598Val
|
|
XM_011535920.2:c.1889G>T
|
XP_011534222.1:p.Gly630Val
|
|
XM_011535921.2:c.1775G>T
|
XP_011534223.1:p.Gly592Val
|
|
XM_011535923.2:c.959G>T
|
XP_011534225.1:p.Gly320Val
|
|
XM_017010991.1:c.1289G>T
|
XP_016866480.1:p.Gly430Val
|
|
XM_017010992.1:c.1289G>T
|
XP_016866481.1:p.Gly430Val
|
|
XM_017010993.1:c.1289G>T
|
XP_016866482.1:p.Gly430Val
|
|
XM_017010994.1:c.1289G>T
|
XP_016866483.1:p.Gly430Val
|
|
NM_018013.4:c.1736G>T
MANE Select
|
NP_060483.3:p.Gly579Val
|
|