ENST00000375448.4:c.1154T>G
MANE Select
|
ENSP00000364597.4:p.Met385Arg
|
|
ENST00000468945.1:n.213T>G
|
|
|
ENST00000487048.5:n.121T>G
|
|
|
NM_012387.2:c.1154T>G
|
NP_036519.2:p.Met385Arg
|
|
XM_011541150.1:c.968T>G
|
XP_011539452.1:p.Met323Arg
|
|
XM_011541151.1:c.1154T>G
|
XP_011539453.1:p.Met385Arg
|
|
XM_011541152.1:c.617T>G
|
XP_011539454.1:p.Met206Arg
|
|
XM_011541153.1:c.1154T>G
|
XP_011539455.1:p.Met385Arg
|
|
XM_011541154.1:c.1154T>G
|
XP_011539456.1:p.Met385Arg
|
|
XM_011541155.1:c.1154T>G
|
XP_011539457.1:p.Met385Arg
|
|
XM_011541156.1:c.1154T>G
|
XP_011539458.1:p.Met385Arg
|
|
XM_011541157.1:c.263T>G
|
XP_011539459.1:p.Met88Arg
|
|
XM_011541154.2:c.1154T>G
|
XP_011539456.1:p.Met385Arg
|
|
NM_012387.3:c.1154T>G
MANE Select
|
NP_036519.2:p.Met385Arg
|
|