|
ENST00000378444.9:c.4111C>T
MANE Select
|
ENSP00000367705.4:p.Gln1371Ter
|
|
|
ENST00000406200.4:c.4111C>T
|
ENSP00000384485.3:p.Gln1371Ter
|
|
|
ENST00000413905.6:c.4009C>T
|
ENSP00000408006.2:p.Gln1337Ter
|
|
|
ENST00000427012.3:c.4057C>T
|
ENSP00000403823.3:p.Gln1353Ter
|
|
|
ENST00000442018.6:c.4111C>T
|
ENSP00000387552.2:p.Gln1371Ter
|
|
|
ENST00000615339.2:c.4111C>T
|
ENSP00000483217.2:p.Gln1371Ter
|
|
|
ENST00000672922.2:c.4111C>T
|
ENSP00000499892.2:p.Gln1371Ter
|
|
|
ENST00000673391.1:c.4009C>T
|
ENSP00000500446.1:p.Gln1337Ter
|
|
|
ENST00000679513.1:c.4111C>T
|
ENSP00000505761.1:p.Gln1371Ter
|
|
|
ENST00000680831.1:c.4111C>T
|
ENSP00000505507.1:p.Gln1371Ter
|
|
|
ENST00000342274.8:c.4009C>T
|
ENSP00000345923.4:p.Gln1337Ter
|
|
|
ENST00000378444.8:c.4111C>T
|
ENSP00000367705.4:p.Gln1371Ter
|
|
|
ENST00000378455.8:c.3955C>T
|
ENSP00000367716.4:p.Gln1319Ter
|
|
|
ENST00000378463.5:c.640C>T
|
ENSP00000367724.1:p.Gln214Ter
|
|
|
ENST00000397354.7:c.4009C>T
|
ENSP00000380512.3:p.Gln1337Ter
|
|
|
ENST00000413905.5:c.721C>T
|
ENSP00000408006.1:p.Gln241Ter
|
|
|
ENST00000427012.1:c.195C>T
|
|
|
|
ENST00000442018.5:c.130C>T
|
ENSP00000387552.1:p.Gln44Ter
|
|
|
NM_001123383.1:c.4009C>T , LRG_627t1:c.4009C>T
|
NP_001116855.1:p.Gln1337Ter
|
|
|
NM_001123384.1:c.3955C>T
|
NP_001116856.1:p.Gln1319Ter
|
|
|
NM_001123385.1:c.4111C>T , LRG_627t2:c.4111C>T
|
NP_001116857.1:p.Gln1371Ter
|
|
|
NM_017745.5:c.4009C>T
|
NP_060215.4:p.Gln1337Ter
|
|
|
XM_005272616.1:c.4111C>T
|
XP_005272673.1:p.Gln1371Ter
|
|
|
XM_005272618.2:c.4111C>T
|
XP_005272675.1:p.Gln1371Ter
|
|
|
XM_005272619.3:c.4057C>T
|
XP_005272676.1:p.Gln1353Ter
|
|
|
XM_005272620.3:c.3955C>T
|
XP_005272677.1:p.Gln1319Ter
|
|
|
XM_006724536.2:c.4111C>T
|
XP_006724599.1:p.Gln1371Ter
|
|
|
XM_011543929.1:c.4111C>T
|
XP_011542231.1:p.Gln1371Ter
|
|
|
XM_011543930.1:c.4111C>T
|
XP_011542232.1:p.Gln1371Ter
|
|
|
XM_011543931.1:c.4111C>T
|
XP_011542233.1:p.Gln1371Ter
|
|
|
XM_005272618.3:c.4111C>T
|
XP_005272675.1:p.Gln1371Ter
|
|
|
XM_005272619.4:c.4057C>T
|
XP_005272676.1:p.Gln1353Ter
|
|
|
XM_005272620.4:c.3955C>T
|
XP_005272677.1:p.Gln1319Ter
|
|
|
XM_006724536.3:c.4111C>T
|
XP_006724599.1:p.Gln1371Ter
|
|
|
XM_011543929.2:c.4111C>T
|
XP_011542231.1:p.Gln1371Ter
|
|
|
XM_011543931.2:c.4111C>T
|
XP_011542233.1:p.Gln1371Ter
|
|
|
XM_017029615.1:c.4009C>T
|
XP_016885104.1:p.Gln1337Ter
|
|
|
XM_017029616.2:c.4111C>T
|
XP_016885105.1:p.Gln1371Ter
|
|
|
NM_001123384.2:c.3955C>T
|
NP_001116856.1:p.Gln1319Ter
|
|
|
NM_001123385.2:c.4111C>T
MANE Select
|
NP_001116857.1:p.Gln1371Ter
|
|
|
NM_017745.6:c.4009C>T
|
NP_060215.4:p.Gln1337Ter
|
|
