ENST00000233190.11:c.822G>T
MANE Select
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ENSP00000233190.5:p.Leu274Phe
|
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ENST00000233190.10:c.822G>T
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ENSP00000233190.5:p.Leu274Phe
|
|
ENST00000423725.5:c.651G>T
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ENSP00000397760.1:p.Leu217Phe
|
|
ENST00000432169.5:c.489G>T
|
ENSP00000409689.1:p.Leu163Phe
|
|
ENST00000440274.5:c.714G>T
|
ENSP00000409766.1:p.Leu238Phe
|
|
ENST00000449699.5:c.822G>T
|
ENSP00000399912.1:p.Leu274Phe
|
|
ENST00000455934.6:c.864G>T
|
ENSP00000392709.2:p.Leu288Phe
|
|
ENST00000457011.5:c.474G>T
|
ENSP00000400976.1:p.Leu158Phe
|
|
NM_001199981.1:c.714G>T
|
NP_001186910.1:p.Leu238Phe
|
|
NM_001199982.1:c.489G>T
|
NP_001186911.1:p.Leu163Phe
|
|
NM_001199983.1:c.651G>T
|
NP_001186912.1:p.Leu217Phe
|
|
NM_001199984.1:c.864G>T
|
NP_001186913.1:p.Leu288Phe
|
|
NM_005006.6:c.822G>T
|
NP_004997.4:p.Leu274Phe
|
|
XM_017004188.2:c.63G>T
|
XP_016859677.1:p.Leu21Phe
|
|
NM_001199981.2:c.714G>T
|
NP_001186910.1:p.Leu238Phe
|
|
NM_001199982.2:c.489G>T
|
NP_001186911.1:p.Leu163Phe
|
|
NM_001199983.2:c.651G>T
|
NP_001186912.1:p.Leu217Phe
|
|
NM_005006.7:c.822G>T
MANE Select
|
NP_004997.4:p.Leu274Phe
|
|
NM_001199984.2:c.864G>T
|
NP_001186913.1:p.Leu288Phe
|
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