ENST00000650516.2:c.1770G>T
|
ENSP00000498052.2:p.Leu590Phe
|
|
ENST00000343257.7:c.1770G>T
MANE Select
|
ENSP00000339867.2:p.Leu590Phe
|
|
ENST00000432192.6:c.1594G>T
|
|
|
ENST00000343257.6:c.1770G>T
|
ENSP00000339867.2:p.Leu590Phe
|
|
NM_000083.2:c.1770G>T
|
NP_000074.2:p.Leu590Phe
|
|
NR_046453.1:n.1710G>T
|
|
|
XM_011515781.1:c.1794G>T
|
XP_011514083.1:p.Leu598Phe
|
|
XM_011515782.1:c.516G>T
|
XP_011514084.1:p.Leu172Phe
|
|
XM_011515782.2:c.516G>T
|
XP_011514084.1:p.Leu172Phe
|
|
XM_017011739.1:c.1344G>T
|
XP_016867228.1:p.Leu448Phe
|
|
XM_017011740.1:c.1320G>T
|
XP_016867229.1:p.Leu440Phe
|
|
NM_000083.3:c.1770G>T
MANE Select
|
NP_000074.3:p.Leu590Phe
|
|
NR_046453.2:n.1725G>T
|
|
|