ENST00000373563.9:c.1843G>T
MANE Select
|
ENSP00000362664.5:p.Glu615Ter
|
|
ENST00000676848.1:c.1189G>T
|
ENSP00000503313.1:p.Glu397Ter
|
|
ENST00000677450.1:c.1324G>T
|
ENSP00000503420.1:p.Glu442Ter
|
|
ENST00000677591.1:c.1099G>T
|
ENSP00000503061.1:p.Glu367Ter
|
|
ENST00000678230.1:c.1336G>T
|
ENSP00000504272.1:p.Glu446Ter
|
|
ENST00000678339.1:c.1099G>T
|
ENSP00000503437.1:p.Glu367Ter
|
|
ENST00000678466.1:c.1099G>T
|
ENSP00000504219.1:p.Glu367Ter
|
|
ENST00000678885.1:c.1099G>T
|
ENSP00000503563.1:p.Glu367Ter
|
|
ENST00000373563.8:c.1843G>T
|
ENSP00000362664.4:p.Glu615Ter
|
|
ENST00000409196.7:c.1825G>T
|
ENSP00000387070.3:p.Glu609Ter
|
|
ENST00000409451.7:c.1906G>T
|
ENSP00000387170.3:p.Glu636Ter
|
|
ENST00000409480.5:c.1909G>T
|
ENSP00000386765.1:p.Glu637Ter
|
|
ENST00000409547.5:c.1843G>T
|
ENSP00000386537.1:p.Glu615Ter
|
|
ENST00000423659.5:c.1672G>T
|
ENSP00000404195.1:p.Glu558Ter
|
|
ENST00000440945.5:c.1825G>T
|
ENSP00000410297.1:p.Glu609Ter
|
|
ENST00000482952.5:n.81G>T
|
|
|
ENST00000629305.2:c.1909G>T
|
ENSP00000487548.1:p.Glu637Ter
|
|
NM_001103146.1:c.1843G>T
|
NP_001096616.1:p.Glu615Ter
|
|
NM_001103147.1:c.1906G>T
|
NP_001096617.1:p.Glu636Ter
|
|
NM_001103148.1:c.1825G>T
|
NP_001096618.1:p.Glu609Ter
|
|
NM_015575.3:c.1843G>T
|
NP_056390.2:p.Glu615Ter
|
|
NR_103492.1:n.1956G>T
|
|
|
NM_001103146.3:c.1843G>T
MANE Select
|
NP_001096616.1:p.Glu615Ter
|
|
NM_001103147.2:c.1906G>T
|
NP_001096617.1:p.Glu636Ter
|
|
NM_001103148.2:c.1825G>T
|
NP_001096618.1:p.Glu609Ter
|
|
NM_015575.4:c.1843G>T
|
NP_056390.2:p.Glu615Ter
|
|