ENST00000282516.13:c.7077T>G
MANE Select
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ENSP00000282516.8:p.Ala2359=
|
|
ENST00000652901.1:c.7077T>G
|
ENSP00000499536.1:p.Ala2359=
|
|
ENST00000282516.12:c.7077T>G
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ENSP00000282516.8:p.Ala2359=
|
|
ENST00000448238.2:c.7077T>G
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ENSP00000406266.2:p.Ala2359=
|
|
ENST00000514335.1:n.959T>G
|
|
|
ENST00000621733.1:c.1-12198T>G
|
ENSP00000480694.1:n.1-12198T>G
|
|
NM_015384.4:c.7077T>G
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NP_056199.2:p.Ala2359=
|
|
NM_133433.3:c.7077T>G
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NP_597677.2:p.Ala2359=
|
|
XM_005248280.2:c.7077T>G
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XP_005248337.1:p.Ala2359=
|
|
XM_005248282.3:c.6333T>G
|
XP_005248339.2:p.Ala2111=
|
|
XM_006714467.2:c.7077T>G
|
XP_006714530.1:p.Ala2359=
|
|
XM_006714468.1:c.6879T>G
|
XP_006714531.1:p.Ala2293=
|
|
XM_011514014.1:c.6696T>G
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XP_011512316.1:p.Ala2232=
|
|
XM_011514015.1:c.7077T>G
|
XP_011512317.1:p.Ala2359=
|
|
XM_005248280.3:c.7077T>G
|
XP_005248337.1:p.Ala2359=
|
|
XM_005248282.5:c.6417T>G
|
XP_005248339.3:p.Ala2139=
|
|
XM_006714468.2:c.6879T>G
|
XP_006714531.1:p.Ala2293=
|
|
XM_017009329.1:c.7077T>G
|
XP_016864818.1:p.Ala2359=
|
|
XM_017009330.2:c.5460T>G
|
XP_016864819.1:p.Ala1820=
|
|
XM_017009331.1:c.5451T>G
|
XP_016864820.1:p.Ala1817=
|
|
NM_133433.4:c.7077T>G
MANE Select
|
NP_597677.2:p.Ala2359=
|
|
NM_015384.5:c.7077T>G
|
NP_056199.2:p.Ala2359=
|
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