ENST00000642683.1:c.687G>C
|
ENSP00000495376.1:p.Met229Ile
|
|
ENST00000643672.1:c.684G>C
|
ENSP00000494532.1:p.Met228Ile
|
|
ENST00000645280.1:c.681G>C
|
ENSP00000496690.1:p.Met227Ile
|
|
ENST00000648579.1:c.*32G>C
|
ENSP00000497638.1:n.*32G>C
|
|
ENST00000650617.1:c.735G>C
MANE Select
|
ENSP00000497532.1:p.Met245Ile
|
|
ENST00000273158.8:c.735G>C
|
ENSP00000273158.3:p.Met245Ile
|
|
NM_017875.2:c.735G>C
|
NP_060345.2:p.Met245Ile
|
|
XM_006713214.1:c.723G>C
|
XP_006713277.1:p.Met241Ile
|
|
XM_011533869.1:c.717G>C
|
XP_011532171.1:p.Met239Ile
|
|
XM_011533870.1:c.684G>C
|
XP_011532172.1:p.Met228Ile
|
|
XM_011533871.1:c.555G>C
|
XP_011532173.1:p.Met185Ile
|
|
NM_001354798.1:c.626-1879G>C
|
NP_001341727.1:n.626-1879G>C
|
|
NM_017875.4:c.735G>C
MANE Select
|
NP_060345.2:p.Met245Ile
|
|
XM_006713214.2:c.723G>C
|
XP_006713277.1:p.Met241Ile
|
|
XM_011533869.2:c.717G>C
|
XP_011532171.1:p.Met239Ile
|
|
XM_024453611.1:c.681G>C
|
XP_024309379.1:p.Met227Ile
|
|
NM_001354798.2:c.626-1879G>C
|
NP_001341727.1:n.626-1879G>C
|
|