|
NM_032119.4:c.14605C>T
MANE Select
|
NP_115495.3:p.Leu4869Phe
|
|
ENST00000405460.9:c.14605C>T
MANE Select
|
ENSP00000384582.2:p.Leu4869Phe
|
|
NM_032119.3:c.14605C>T
|
NP_115495.3:p.Leu4869Phe
|
|
NR_003149.1:n.14618C>T
|
|
|
NR_003149.2:n.14621C>T
|
|
|
ENST00000405460.6:c.14605C>T
|
ENSP00000384582.2:p.Leu4869Phe
|
|
ENST00000425867.2:c.1588C>T
|
ENSP00000392618.2:p.Leu530Phe
|
|
ENST00000425867.3:c.3559C>T
|
ENSP00000392618.3:p.Leu1187Phe
|
|
ENST00000638510.1:n.1872C>T
|
|
|
ENST00000638585.1:n.371C>T
|
|
|
ENST00000639431.1:c.265+126617C>T
|
ENSP00000491057.1:n.265+126617C>T
|
|
ENST00000640407.1:c.1015C>T
|
ENSP00000491425.1:p.Leu339Phe
|
|
XM_011543675.1:c.14602C>T
|
XP_011541977.1:p.Leu4868Phe
|
|
XM_011543676.1:c.14524C>T
|
XP_011541978.1:p.Leu4842Phe
|
|
XM_011543677.1:c.11908C>T
|
XP_011541979.1:p.Leu3970Phe
|
|
XM_011543678.1:c.14605C>T
|
XP_011541980.1:p.Leu4869Phe
|
|
XM_017009963.2:c.14626C>T
|
XP_016865452.1:p.Leu4876Phe
|
|
XM_017009964.2:c.14623C>T
|
XP_016865453.1:p.Leu4875Phe
|
|
XM_017009965.1:c.14623C>T
|
XP_016865454.1:p.Leu4875Phe
|
|
XM_017009966.2:c.14545C>T
|
XP_016865455.1:p.Leu4849Phe
|
|
XM_017009967.1:c.14530C>T
|
XP_016865456.1:p.Leu4844Phe
|
|
XM_017009968.2:c.14626C>T
|
XP_016865457.1:p.Leu4876Phe
|
|
XM_017009969.2:c.14626C>T
|
XP_016865458.1:p.Leu4876Phe
|
|
XM_017009970.2:c.14626C>T
|
XP_016865459.1:p.Leu4876Phe
|
|
XM_017009971.2:c.14626C>T
|
XP_016865460.1:p.Leu4876Phe
|
|
XM_017009972.1:c.7744C>T
|
XP_016865461.1:p.Leu2582Phe
|
|
XM_017009973.1:c.7723C>T
|
XP_016865462.1:p.Leu2575Phe
|