ENST00000405460.9:c.11532A>C
MANE Select
|
ENSP00000384582.2:p.Ile3844=
|
|
ENST00000425867.3:c.663A>C
|
ENSP00000392618.3:p.Ile221=
|
|
ENST00000639431.1:c.265+78928A>C
|
ENSP00000491057.1:n.265+78928A>C
|
|
ENST00000640374.1:n.4676A>C
|
|
|
ENST00000640464.1:n.1951A>C
|
|
|
ENST00000405460.6:c.11532A>C
|
ENSP00000384582.2:p.Ile3844=
|
|
ENST00000509621.1:c.4229A>C
|
|
|
NM_032119.3:c.11532A>C
|
NP_115495.3:p.Ile3844=
|
|
NR_003149.1:n.11545A>C
|
|
|
XM_011543675.1:c.11529A>C
|
XP_011541977.1:p.Ile3843=
|
|
XM_011543676.1:c.11451A>C
|
XP_011541978.1:p.Ile3817=
|
|
XM_011543677.1:c.8835A>C
|
XP_011541979.1:p.Ile2945=
|
|
XM_011543678.1:c.11532A>C
|
XP_011541980.1:p.Ile3844=
|
|
NM_032119.4:c.11532A>C
MANE Select
|
NP_115495.3:p.Ile3844=
|
|
XM_017009963.2:c.11553A>C
|
XP_016865452.1:p.Ile3851=
|
|
XM_017009964.2:c.11550A>C
|
XP_016865453.1:p.Ile3850=
|
|
XM_017009965.1:c.11550A>C
|
XP_016865454.1:p.Ile3850=
|
|
XM_017009966.2:c.11472A>C
|
XP_016865455.1:p.Ile3824=
|
|
XM_017009967.1:c.11457A>C
|
XP_016865456.1:p.Ile3819=
|
|
XM_017009968.2:c.11553A>C
|
XP_016865457.1:p.Ile3851=
|
|
XM_017009969.2:c.11553A>C
|
XP_016865458.1:p.Ile3851=
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|
XM_017009970.2:c.11553A>C
|
XP_016865459.1:p.Ile3851=
|
|
XM_017009971.2:c.11553A>C
|
XP_016865460.1:p.Ile3851=
|
|
XM_017009972.1:c.4671A>C
|
XP_016865461.1:p.Ile1557=
|
|
XM_017009973.1:c.4650A>C
|
XP_016865462.1:p.Ile1550=
|
|
NR_003149.2:n.11548A>C
|
|
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