ENST00000650516.2:c.2816C>G
|
ENSP00000498052.2:p.Pro939Arg
|
|
ENST00000343257.7:c.2816C>G
MANE Select
|
ENSP00000339867.2:p.Pro939Arg
|
|
ENST00000343257.6:c.2816C>G
|
ENSP00000339867.2:p.Pro939Arg
|
|
NM_000083.2:c.2816C>G
|
NP_000074.2:p.Pro939Arg
|
|
NR_046453.1:n.2756C>G
|
|
|
XM_011515781.1:c.2840C>G
|
XP_011514083.1:p.Pro947Arg
|
|
XM_011515782.1:c.1562C>G
|
XP_011514084.1:p.Pro521Arg
|
|
XM_011515782.2:c.1562C>G
|
XP_011514084.1:p.Pro521Arg
|
|
XM_017011739.1:c.2390C>G
|
XP_016867228.1:p.Pro797Arg
|
|
XM_017011740.1:c.2366C>G
|
XP_016867229.1:p.Pro789Arg
|
|
NM_000083.3:c.2816C>G
MANE Select
|
NP_000074.3:p.Pro939Arg
|
|
NR_046453.2:n.2771C>G
|
|
|