ENST00000302850.10:c.3252T>A
MANE Select
|
ENSP00000303830.4:p.His1084Gln
|
|
ENST00000302850.9:c.3252T>A
|
ENSP00000303830.4:p.His1084Gln
|
|
ENST00000341500.9:c.3216T>A
|
ENSP00000342838.4:p.His1072Gln
|
|
ENST00000593970.1:n.98T>A
|
|
|
NM_000208.2:c.3252T>A
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NP_000199.2:p.His1084Gln
|
|
NM_000208.3:c.3252T>A
|
NP_000199.2:p.His1084Gln
|
|
NM_001079817.1:c.3216T>A
|
NP_001073285.1:p.His1072Gln
|
|
NM_001079817.2:c.3216T>A
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NP_001073285.1:p.His1072Gln
|
|
XM_011527988.1:c.3327T>A
|
XP_011526290.1:p.His1109Gln
|
|
XM_011527989.1:c.3291T>A
|
XP_011526291.1:p.His1097Gln
|
|
XM_011527988.2:c.3249T>A
|
XP_011526290.2:p.His1083Gln
|
|
XM_011527989.3:c.3213T>A
|
XP_011526291.2:p.His1071Gln
|
|
NM_000208.4:c.3252T>A
MANE Select
|
NP_000199.2:p.His1084Gln
|
|
NM_001079817.3:c.3216T>A
|
NP_001073285.1:p.His1072Gln
|
|