ENST00000405460.9:c.10577T>G
MANE Select
|
ENSP00000384582.2:p.Met3526Arg
|
|
ENST00000639431.1:c.265+68864T>G
|
ENSP00000491057.1:n.265+68864T>G
|
|
ENST00000640374.1:n.3721T>G
|
|
|
ENST00000640464.1:n.996T>G
|
|
|
ENST00000405460.6:c.10577T>G
|
ENSP00000384582.2:p.Met3526Arg
|
|
ENST00000509621.1:c.3274T>G
|
|
|
NM_032119.3:c.10577T>G
|
NP_115495.3:p.Met3526Arg
|
|
NR_003149.1:n.10590T>G
|
|
|
XM_011543675.1:c.10574T>G
|
XP_011541977.1:p.Met3525Arg
|
|
XM_011543676.1:c.10496T>G
|
XP_011541978.1:p.Met3499Arg
|
|
XM_011543677.1:c.7880T>G
|
XP_011541979.1:p.Met2627Arg
|
|
XM_011543678.1:c.10577T>G
|
XP_011541980.1:p.Met3526Arg
|
|
XM_011543679.1:c.10577T>G
|
XP_011541981.1:p.Met3526Arg
|
|
NM_032119.4:c.10577T>G
MANE Select
|
NP_115495.3:p.Met3526Arg
|
|
XM_017009963.2:c.10598T>G
|
XP_016865452.1:p.Met3533Arg
|
|
XM_017009964.2:c.10595T>G
|
XP_016865453.1:p.Met3532Arg
|
|
XM_017009965.1:c.10595T>G
|
XP_016865454.1:p.Met3532Arg
|
|
XM_017009966.2:c.10517T>G
|
XP_016865455.1:p.Met3506Arg
|
|
XM_017009967.1:c.10502T>G
|
XP_016865456.1:p.Met3501Arg
|
|
XM_017009968.2:c.10598T>G
|
XP_016865457.1:p.Met3533Arg
|
|
XM_017009969.2:c.10598T>G
|
XP_016865458.1:p.Met3533Arg
|
|
XM_017009970.2:c.10598T>G
|
XP_016865459.1:p.Met3533Arg
|
|
XM_017009971.2:c.10598T>G
|
XP_016865460.1:p.Met3533Arg
|
|
XM_017009972.1:c.3716T>G
|
XP_016865461.1:p.Met1239Arg
|
|
XM_017009973.1:c.3695T>G
|
XP_016865462.1:p.Met1232Arg
|
|
XM_017009974.2:c.10598T>G
|
XP_016865463.1:p.Met3533Arg
|
|
NR_003149.2:n.10593T>G
|
|
|