ENST00000650516.2:c.2702C>G
|
ENSP00000498052.2:p.Pro901Arg
|
|
ENST00000343257.7:c.2702C>G
MANE Select
|
ENSP00000339867.2:p.Pro901Arg
|
|
ENST00000432192.6:c.2526C>G
|
|
|
ENST00000343257.6:c.2702C>G
|
ENSP00000339867.2:p.Pro901Arg
|
|
NM_000083.2:c.2702C>G
|
NP_000074.2:p.Pro901Arg
|
|
NR_046453.1:n.2642C>G
|
|
|
XM_011515781.1:c.2726C>G
|
XP_011514083.1:p.Pro909Arg
|
|
XM_011515782.1:c.1448C>G
|
XP_011514084.1:p.Pro483Arg
|
|
XM_011515782.2:c.1448C>G
|
XP_011514084.1:p.Pro483Arg
|
|
XM_017011739.1:c.2276C>G
|
XP_016867228.1:p.Pro759Arg
|
|
XM_017011740.1:c.2252C>G
|
XP_016867229.1:p.Pro751Arg
|
|
NM_000083.3:c.2702C>G
MANE Select
|
NP_000074.3:p.Pro901Arg
|
|
NR_046453.2:n.2657C>G
|
|
|