ENST00000642683.1:c.596T>A
|
ENSP00000495376.1:p.Leu199His
|
|
ENST00000643672.1:c.593T>A
|
ENSP00000494532.1:p.Leu198His
|
|
ENST00000645280.1:c.590T>A
|
ENSP00000496690.1:p.Leu197His
|
|
ENST00000648579.1:c.722-22T>A
|
ENSP00000497638.1:n.722-22T>A
|
|
ENST00000650617.1:c.644T>A
MANE Select
|
ENSP00000497532.1:p.Leu215His
|
|
ENST00000273158.8:c.644T>A
|
ENSP00000273158.3:p.Leu215His
|
|
NM_017875.2:c.644T>A
|
NP_060345.2:p.Leu215His
|
|
XM_006713214.1:c.632T>A
|
XP_006713277.1:p.Leu211His
|
|
XM_011533869.1:c.626T>A
|
XP_011532171.1:p.Leu209His
|
|
XM_011533870.1:c.593T>A
|
XP_011532172.1:p.Leu198His
|
|
XM_011533871.1:c.464T>A
|
XP_011532173.1:p.Leu155His
|
|
NM_001354798.1:c.626-1970T>A
|
NP_001341727.1:n.626-1970T>A
|
|
NM_017875.4:c.644T>A
MANE Select
|
NP_060345.2:p.Leu215His
|
|
XM_006713214.2:c.632T>A
|
XP_006713277.1:p.Leu211His
|
|
XM_011533869.2:c.626T>A
|
XP_011532171.1:p.Leu209His
|
|
XM_024453611.1:c.590T>A
|
XP_024309379.1:p.Leu197His
|
|
NM_001354798.2:c.626-1970T>A
|
NP_001341727.1:n.626-1970T>A
|
|