ENST00000407991.3:c.1255G>T
MANE Select
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ENSP00000385026.1:p.Glu419Ter
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ENST00000240132.7:c.1210G>T
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ENSP00000240132.2:p.Glu404Ter
|
|
ENST00000407991.2:c.1255G>T
|
ENSP00000385026.1:p.Glu419Ter
|
|
ENST00000520600.1:n.290-1434G>T
|
|
|
ENST00000520933.7:c.1189G>T
|
ENSP00000429616.2:p.Glu397Ter
|
|
ENST00000523695.5:c.*657G>T
|
ENSP00000430612.1:n.*657G>T
|
|
NM_000742.3:c.1255G>T
|
NP_000733.2:p.Glu419Ter
|
|
NM_001282455.1:c.1210G>T
|
NP_001269384.1:p.Glu404Ter
|
|
XM_005273397.1:c.778G>T
|
XP_005273454.1:p.Glu260Ter
|
|
XM_006716282.1:c.1255G>T
|
XP_006716345.1:p.Glu419Ter
|
|
XM_011544388.1:c.1255G>T
|
XP_011542690.1:p.Glu419Ter
|
|
XM_011544389.1:c.661G>T
|
XP_011542691.1:p.Glu221Ter
|
|
NM_001347705.1:c.778G>T
|
NP_001334634.1:p.Glu260Ter
|
|
NM_001347706.1:c.778G>T
|
NP_001334635.1:p.Glu260Ter
|
|
NM_001347707.1:c.661G>T
|
NP_001334636.1:p.Glu221Ter
|
|
NM_001347708.1:c.661G>T
|
NP_001334637.1:p.Glu221Ter
|
|
XM_011544389.2:c.661G>T
|
XP_011542691.1:p.Glu221Ter
|
|
NM_000742.4:c.1255G>T
MANE Select
|
NP_000733.2:p.Glu419Ter
|
|
NM_001282455.2:c.1210G>T
|
NP_001269384.1:p.Glu404Ter
|
|
NM_001347705.2:c.778G>T
|
NP_001334634.1:p.Glu260Ter
|
|
NM_001347706.2:c.778G>T
|
NP_001334635.1:p.Glu260Ter
|
|
NM_001347707.2:c.661G>T
|
NP_001334636.1:p.Glu221Ter
|
|
NM_001347708.2:c.661G>T
|
NP_001334637.1:p.Glu221Ter
|
|