ENST00000355832.10:c.3816G>T
MANE Select
|
ENSP00000348089.5:p.Met1272Ile
|
|
ENST00000679552.1:n.887G>T
|
|
|
ENST00000679871.1:n.962G>T
|
|
|
ENST00000679974.1:n.865G>T
|
|
|
ENST00000681632.1:n.5219G>T
|
|
|
ENST00000681659.1:c.3657G>T
|
ENSP00000505631.1:p.Met1219Ile
|
|
ENST00000355832.9:c.3816G>T
|
ENSP00000348089.5:p.Met1272Ile
|
|
ENST00000465653.1:n.138G>T
|
|
|
ENST00000623073.3:c.*2112G>T
|
ENSP00000485650.1:n.*2112G>T
|
|
ENST00000623115.3:c.1926G>T
|
ENSP00000485321.1:p.Met642Ile
|
|
ENST00000624341.3:c.1648G>T
|
|
|
NM_000124.3:c.3816G>T
|
NP_000115.1:p.Met1272Ile
|
|
XR_945953.1:n.243-10046C>A
|
|
|
NM_001346440.1:c.3816G>T
|
NP_001333369.1:p.Met1272Ile
|
|
NM_000124.4:c.3816G>T
MANE Select
|
NP_000115.1:p.Met1272Ile
|
|
NM_001346440.2:c.3816G>T
|
NP_001333369.1:p.Met1272Ile
|
|