ENST00000400521.7:c.1174T>C
MANE Select
|
ENSP00000383365.1:p.Tyr392His
|
|
ENST00000400518.5:c.1084T>C
|
ENSP00000383362.1:p.Tyr362His
|
|
ENST00000400519.6:c.1171T>C
|
ENSP00000383363.1:p.Tyr391His
|
|
ENST00000400521.6:c.1174T>C
|
ENSP00000383365.1:p.Tyr392His
|
|
ENST00000400525.6:c.1105T>C
|
ENSP00000383369.3:p.Tyr369His
|
|
ENST00000462330.5:c.97T>C
|
ENSP00000485603.2:p.Tyr33His
|
|
ENST00000462843.2:c.124T>C
|
ENSP00000485466.2:p.Tyr42His
|
|
ENST00000474308.5:c.1117T>C
|
ENSP00000485665.1:p.Tyr373His
|
|
ENST00000485358.5:c.142T>C
|
ENSP00000485499.2:p.Tyr48His
|
|
ENST00000487165.5:n.1268T>C
|
|
|
ENST00000494454.5:n.1248T>C
|
|
|
ENST00000495655.2:n.718T>C
|
|
|
ENST00000542719.6:c.886T>C
|
ENSP00000485128.2:p.Tyr296His
|
|
ENST00000634471.1:n.244-359T>C
|
|
|
ENST00000634537.1:c.403T>C
|
ENSP00000489208.1:p.Tyr135His
|
|
NM_006440.4:c.1174T>C
|
NP_006431.2:p.Tyr392His
|
|
NM_001352300.1:c.1171T>C
|
NP_001339229.1:p.Tyr391His
|
|
NM_001352301.1:c.1084T>C
|
NP_001339230.1:p.Tyr362His
|
|
NM_001352302.1:c.886T>C
|
NP_001339231.1:p.Tyr296His
|
|
NR_147957.1:n.1306T>C
|
|
|
NM_006440.5:c.1174T>C
MANE Select
|
NP_006431.2:p.Tyr392His
|
|
NM_001352300.2:c.1171T>C
|
NP_001339229.1:p.Tyr391His
|
|
NR_147957.2:n.1132T>C
|
|
|
NM_001352301.2:c.1084T>C
|
NP_001339230.1:p.Tyr362His
|
|
NM_001352302.2:c.886T>C
|
NP_001339231.1:p.Tyr296His
|
|