ENST00000264428.9:c.593A>T
MANE Select
|
ENSP00000264428.4:p.Lys198Met
|
|
ENST00000264428.8:c.593A>T
|
ENSP00000264428.4:p.Lys198Met
|
|
ENST00000506411.5:c.*513A>T
|
ENSP00000422039.1:n.*513A>T
|
|
ENST00000509282.1:c.593A>T
|
ENSP00000427186.1:p.Lys198Met
|
|
ENST00000510970.1:n.400A>T
|
|
|
ENST00000512619.5:c.123-33563A>T
|
ENSP00000425433.1:n.123-33563A>T
|
|
ENST00000541722.5:c.593A>T
|
ENSP00000441873.1:p.Lys198Met
|
|
NM_000824.4:c.593A>T
|
NP_000815.1:p.Lys198Met
|
|
NM_001166060.1:c.593A>T
|
NP_001159532.1:p.Lys198Met
|
|
NM_001166061.1:c.593A>T
|
NP_001159533.1:p.Lys198Met
|
|
XM_011531876.1:c.299A>T
|
XP_011530178.1:p.Lys100Met
|
|
XM_017008034.1:c.299A>T
|
XP_016863523.1:p.Lys100Met
|
|
XM_017008035.2:c.593A>T
|
XP_016863524.1:p.Lys198Met
|
|
XR_001741207.2:n.774A>T
|
|
|
XR_002959723.1:n.774A>T
|
|
|
NM_000824.5:c.593A>T
MANE Select
|
NP_000815.1:p.Lys198Met
|
|
NM_001166060.2:c.593A>T
|
NP_001159532.1:p.Lys198Met
|
|
NM_001166061.2:c.593A>T
|
NP_001159533.1:p.Lys198Met
|
|