ENST00000233190.11:c.831G=
MANE Select
|
ENSP00000233190.5:p.Met277=
|
|
ENST00000233190.10:c.831G=
|
ENSP00000233190.5:p.Met277=
|
|
ENST00000423725.5:c.660G=
|
ENSP00000397760.1:p.Met220=
|
|
ENST00000432169.5:c.498G=
|
ENSP00000409689.1:p.Met166=
|
|
ENST00000440274.5:c.723G=
|
ENSP00000409766.1:p.Met241=
|
|
ENST00000449699.5:c.831G=
|
ENSP00000399912.1:p.Met277=
|
|
ENST00000455934.6:c.873G=
|
ENSP00000392709.2:p.Met291=
|
|
ENST00000457011.5:c.483G=
|
ENSP00000400976.1:p.Met161=
|
|
NM_001199981.1:c.723G=
|
NP_001186910.1:p.Met241=
|
|
NM_001199982.1:c.498G=
|
NP_001186911.1:p.Met166=
|
|
NM_001199983.1:c.660G=
|
NP_001186912.1:p.Met220=
|
|
NM_001199984.1:c.873G=
|
NP_001186913.1:p.Met291=
|
|
NM_005006.6:c.831G=
|
NP_004997.4:p.Met277=
|
|
XM_017004188.2:c.72G=
|
XP_016859677.1:p.Met24=
|
|
NM_001199981.2:c.723G=
|
NP_001186910.1:p.Met241=
|
|
NM_001199982.2:c.498G=
|
NP_001186911.1:p.Met166=
|
|
NM_001199983.2:c.660G=
|
NP_001186912.1:p.Met220=
|
|
NM_005006.7:c.831G=
MANE Select
|
NP_004997.4:p.Met277=
|
|
NM_001199984.2:c.873G=
|
NP_001186913.1:p.Met291=
|
|