ENST00000642683.1:c.697C>T
|
ENSP00000495376.1:p.Pro233Ser
|
|
ENST00000643672.1:c.694C>T
|
ENSP00000494532.1:p.Pro232Ser
|
|
ENST00000645280.1:c.691C>T
|
ENSP00000496690.1:p.Pro231Ser
|
|
ENST00000648579.1:c.*42C>T
|
ENSP00000497638.1:n.*42C>T
|
|
ENST00000650617.1:c.745C>T
MANE Select
|
ENSP00000497532.1:p.Pro249Ser
|
|
ENST00000273158.8:c.745C>T
|
ENSP00000273158.3:p.Pro249Ser
|
|
NM_017875.2:c.745C>T
|
NP_060345.2:p.Pro249Ser
|
|
XM_006713214.1:c.733C>T
|
XP_006713277.1:p.Pro245Ser
|
|
XM_011533869.1:c.727C>T
|
XP_011532171.1:p.Pro243Ser
|
|
XM_011533870.1:c.694C>T
|
XP_011532172.1:p.Pro232Ser
|
|
XM_011533871.1:c.565C>T
|
XP_011532173.1:p.Pro189Ser
|
|
NM_001354798.1:c.626-1869C>T
|
NP_001341727.1:n.626-1869C>T
|
|
NM_017875.4:c.745C>T
MANE Select
|
NP_060345.2:p.Pro249Ser
|
|
XM_006713214.2:c.733C>T
|
XP_006713277.1:p.Pro245Ser
|
|
XM_011533869.2:c.727C>T
|
XP_011532171.1:p.Pro243Ser
|
|
XM_024453611.1:c.691C>T
|
XP_024309379.1:p.Pro231Ser
|
|
NM_001354798.2:c.626-1869C>T
|
NP_001341727.1:n.626-1869C>T
|
|