ENST00000368985.8:c.924A>T
MANE Select
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ENSP00000357981.3:p.Gly308=
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ENST00000448301.7:c.696A>T
|
ENSP00000408414.2:p.Gly232=
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|
ENST00000472977.7:c.924A>T
|
ENSP00000475176.2:p.Gly308=
|
|
ENST00000483930.2:c.*118A>T
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ENSP00000475812.2:n.*118A>T
|
|
ENST00000607427.2:c.924A>T
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ENSP00000475557.2:p.Gly308=
|
|
ENST00000679512.1:c.821A>T
|
ENSP00000505113.1:p.Asp274Val
|
|
ENST00000679898.1:c.651A>T
|
ENSP00000505326.1:p.Gly217=
|
|
ENST00000680288.1:c.774A>T
|
ENSP00000506001.1:p.Gly258=
|
|
ENST00000680311.1:c.*7A>T
|
ENSP00000505020.1:n.*7A>T
|
|
ENST00000680471.1:c.*95A>T
|
ENSP00000506603.1:n.*95A>T
|
|
ENST00000680664.1:c.747A>T
|
ENSP00000506248.1:p.Gly249=
|
|
ENST00000680931.1:c.*274A>T
|
ENSP00000504934.1:n.*274A>T
|
|
ENST00000681357.1:n.314A>T
|
|
|
ENST00000681444.1:c.924A>T
|
ENSP00000505359.1:p.Gly308=
|
|
ENST00000368985.7:c.924A>T
|
ENSP00000357981.3:p.Gly308=
|
|
ENST00000448301.6:c.774A>T
|
ENSP00000408414.1:p.Gly258=
|
|
ENST00000472977.6:c.217A>T
|
|
|
ENST00000483930.1:c.472A>T
|
ENSP00000475812.1:n.472A>T
|
|
NM_001199739.1:c.774A>T
|
NP_001186668.1:p.Gly258=
|
|
NM_004079.4:c.924A>T
|
NP_004070.3:p.Gly308=
|
|
NM_004079.5:c.924A>T
MANE Select
|
NP_004070.3:p.Gly308=
|
|
NM_001199739.2:c.774A>T
|
NP_001186668.1:p.Gly258=
|
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