ENST00000584880.6:c.*408T>A
|
ENSP00000464347.2:n.*408T>A
|
|
ENST00000703608.1:c.*728T>A
|
ENSP00000515392.1:n.*728T>A
|
|
ENST00000703609.1:c.1130T>A
|
ENSP00000515393.1:p.Leu377Ter
|
|
ENST00000703610.1:c.*488T>A
|
ENSP00000515394.1:n.*488T>A
|
|
ENST00000310144.11:c.1211T>A
MANE Select
|
ENSP00000310572.6:p.Leu404Ter
|
|
ENST00000310144.10:c.1211T>A
|
ENSP00000310572.6:p.Leu404Ter
|
|
ENST00000375812.8:c.1187T>A
|
ENSP00000364970.4:p.Leu396Ter
|
|
ENST00000578570.5:n.1621T>A
|
|
|
ENST00000579147.5:n.2526T>A
|
|
|
ENST00000580864.5:c.1187T>A
|
ENSP00000462495.1:p.Leu396Ter
|
|
ENST00000581882.5:c.1187T>A
|
ENSP00000463938.1:p.Leu396Ter
|
|
ENST00000584657.1:n.516T>A
|
|
|
ENST00000585242.5:c.*982T>A
|
ENSP00000463107.1:n.*982T>A
|
|
NM_001199163.1:c.1187T>A
|
NP_001186092.1:p.Leu396Ter
|
|
NM_002805.5:c.1211T>A
|
NP_002796.4:p.Leu404Ter
|
|
XM_006721980.1:c.1211T>A
|
XP_006722043.1:p.Leu404Ter
|
|
XR_934508.1:n.1300T>A
|
|
|
XM_024450840.1:c.1292T>A
|
XP_024306608.1:p.Leu431Ter
|
|
XM_024450841.1:c.1268T>A
|
XP_024306609.1:p.Leu423Ter
|
|
XR_934508.2:n.1287T>A
|
|
|
NM_002805.6:c.1211T>A
MANE Select
|
NP_002796.4:p.Leu404Ter
|
|
NM_001199163.2:c.1187T>A
|
NP_001186092.1:p.Leu396Ter
|
|