ENST00000642683.1:c.736A>T
|
ENSP00000495376.1:p.Ile246Phe
|
|
ENST00000643672.1:c.733A>T
|
ENSP00000494532.1:p.Ile245Phe
|
|
ENST00000645280.1:c.730A>T
|
ENSP00000496690.1:p.Ile244Phe
|
|
ENST00000648579.1:c.*81A>T
|
ENSP00000497638.1:n.*81A>T
|
|
ENST00000650617.1:c.784A>T
MANE Select
|
ENSP00000497532.1:p.Ile262Phe
|
|
ENST00000273158.8:c.784A>T
|
ENSP00000273158.3:p.Ile262Phe
|
|
NM_017875.2:c.784A>T
|
NP_060345.2:p.Ile262Phe
|
|
XM_006713214.1:c.772A>T
|
XP_006713277.1:p.Ile258Phe
|
|
XM_011533869.1:c.766A>T
|
XP_011532171.1:p.Ile256Phe
|
|
XM_011533870.1:c.733A>T
|
XP_011532172.1:p.Ile245Phe
|
|
XM_011533871.1:c.604A>T
|
XP_011532173.1:p.Ile202Phe
|
|
NM_001354798.1:c.626-1830A>T
|
NP_001341727.1:n.626-1830A>T
|
|
NM_017875.4:c.784A>T
MANE Select
|
NP_060345.2:p.Ile262Phe
|
|
XM_006713214.2:c.772A>T
|
XP_006713277.1:p.Ile258Phe
|
|
XM_011533869.2:c.766A>T
|
XP_011532171.1:p.Ile256Phe
|
|
XM_024453611.1:c.730A>T
|
XP_024309379.1:p.Ile244Phe
|
|
NM_001354798.2:c.626-1830A>T
|
NP_001341727.1:n.626-1830A>T
|
|