ENST00000233190.11:c.761T>C
MANE Select
|
ENSP00000233190.5:p.Met254Thr
|
|
ENST00000233190.10:c.761T>C
|
ENSP00000233190.5:p.Met254Thr
|
|
ENST00000423725.5:c.590T>C
|
ENSP00000397760.1:p.Met197Thr
|
|
ENST00000432169.5:c.428T>C
|
ENSP00000409689.1:p.Met143Thr
|
|
ENST00000440274.5:c.653T>C
|
ENSP00000409766.1:p.Met218Thr
|
|
ENST00000449699.5:c.761T>C
|
ENSP00000399912.1:p.Met254Thr
|
|
ENST00000455934.6:c.803T>C
|
ENSP00000392709.2:p.Met268Thr
|
|
ENST00000457011.5:c.413T>C
|
ENSP00000400976.1:p.Met138Thr
|
|
NM_001199981.1:c.653T>C
|
NP_001186910.1:p.Met218Thr
|
|
NM_001199982.1:c.428T>C
|
NP_001186911.1:p.Met143Thr
|
|
NM_001199983.1:c.590T>C
|
NP_001186912.1:p.Met197Thr
|
|
NM_001199984.1:c.803T>C
|
NP_001186913.1:p.Met268Thr
|
|
NM_005006.6:c.761T>C
|
NP_004997.4:p.Met254Thr
|
|
XM_017004188.2:c.2T>C
|
XP_016859677.1:p.Met1Thr
|
|
NM_001199981.2:c.653T>C
|
NP_001186910.1:p.Met218Thr
|
|
NM_001199982.2:c.428T>C
|
NP_001186911.1:p.Met143Thr
|
|
NM_001199983.2:c.590T>C
|
NP_001186912.1:p.Met197Thr
|
|
NM_005006.7:c.761T>C
MANE Select
|
NP_004997.4:p.Met254Thr
|
|
NM_001199984.2:c.803T>C
|
NP_001186913.1:p.Met268Thr
|
|