ENST00000388996.10:c.814C>T
MANE Select
|
ENSP00000373648.3:p.Leu272Phe
|
|
ENST00000521134.6:c.454C>T
|
ENSP00000429799.1:p.Leu152Phe
|
|
ENST00000638588.1:c.487C>T
|
ENSP00000491940.1:p.Leu163Phe
|
|
ENST00000639358.1:c.464C>T
|
|
|
ENST00000639496.1:c.487C>T
|
ENSP00000491165.1:p.Leu163Phe
|
|
ENST00000388996.8:c.814C>T
|
ENSP00000373648.3:p.Leu272Phe
|
|
ENST00000519445.5:c.814C>T
|
ENSP00000428790.1:p.Leu272Phe
|
|
ENST00000519589.1:n.592C>T
|
|
|
ENST00000521134.5:c.454C>T
|
ENSP00000429799.1:p.Leu152Phe
|
|
ENST00000621976.1:c.451C>T
|
ENSP00000482510.1:p.Leu151Phe
|
|
NM_001204824.1:c.454C>T
|
NP_001191753.1:p.Leu152Phe
|
|
NM_004519.3:c.814C>T
|
NP_004510.1:p.Leu272Phe
|
|
XM_005250914.2:c.-343C>T
|
XP_005250971.1:n.-343C>T
|
|
XM_006716555.2:c.106C>T
|
XP_006716618.1:p.Leu36Phe
|
|
XM_011517026.1:c.454C>T
|
XP_011515328.1:p.Leu152Phe
|
|
XM_005250914.3:c.-343C>T
|
XP_005250971.1:n.-343C>T
|
|
XM_006716555.3:c.106C>T
|
XP_006716618.1:p.Leu36Phe
|
|
XM_011517026.2:c.454C>T
|
XP_011515328.1:p.Leu152Phe
|
|
XM_017013400.1:c.592C>T
|
XP_016868889.1:p.Leu198Phe
|
|
NM_004519.4:c.814C>T
MANE Select
|
NP_004510.1:p.Leu272Phe
|
|
NM_001204824.2:c.454C>T
|
NP_001191753.1:p.Leu152Phe
|
|