ENST00000375448.4:c.279G>C
MANE Select
|
ENSP00000364597.4:p.Gln93His
|
|
ENST00000375453.5:c.279G>C
|
ENSP00000364602.1:p.Gln93His
|
|
NM_012387.2:c.279G>C
|
NP_036519.2:p.Gln93His
|
|
XM_011541150.1:c.279G>C
|
XP_011539452.1:p.Gln93His
|
|
XM_011541151.1:c.279G>C
|
XP_011539453.1:p.Gln93His
|
|
XM_011541153.1:c.279G>C
|
XP_011539455.1:p.Gln93His
|
|
XM_011541154.1:c.279G>C
|
XP_011539456.1:p.Gln93His
|
|
XM_011541155.1:c.279G>C
|
XP_011539457.1:p.Gln93His
|
|
XM_011541156.1:c.279G>C
|
XP_011539458.1:p.Gln93His
|
|
XM_011541154.2:c.279G>C
|
XP_011539456.1:p.Gln93His
|
|
NM_012387.3:c.279G>C
MANE Select
|
NP_036519.2:p.Gln93His
|
|