ENST00000307363.10:c.1826T>C
MANE Select
|
ENSP00000306920.4:p.Met609Thr
|
|
ENST00000307363.9:c.1826T>C
|
ENSP00000306920.4:p.Met609Thr
|
|
ENST00000307377.12:c.1433T>C
|
ENSP00000305920.8:p.Met478Thr
|
|
ENST00000399402.7:c.1736T>C
|
ENSP00000382333.2:p.Met579Thr
|
|
NM_000404.2:c.1826T>C
|
NP_000395.2:p.Met609Thr
|
|
NM_000404.3:c.1826T>C
|
NP_000395.2:p.Met609Thr
|
|
NM_001079811.1:c.1736T>C
|
NP_001073279.1:p.Met579Thr
|
|
NM_001079811.2:c.1736T>C
|
NP_001073279.1:p.Met579Thr
|
|
NM_001135602.1:c.1433T>C
|
NP_001129074.1:p.Met478Thr
|
|
NM_001135602.2:c.1433T>C
|
NP_001129074.1:p.Met478Thr
|
|
NM_001317040.1:c.1970T>C
|
NP_001303969.1:p.Met657Thr
|
|
NM_000404.4:c.1826T>C
MANE Select
|
NP_000395.3:p.Met609Thr
|
|
NM_001079811.3:c.1736T>C
|
NP_001073279.2:p.Met579Thr
|
|
NM_001135602.3:c.1433T>C
|
NP_001129074.2:p.Met478Thr
|
|
NM_001317040.2:c.1970T>C
|
NP_001303969.2:p.Met657Thr
|
|
NM_001393580.1:c.1734+16803T>C
|
NP_001380509.1:n.1734+16803T>C
|
|