ENST00000593993.7:c.1965A>G
MANE Select
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ENSP00000472165.2:p.Gly655=
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ENST00000593993.6:c.1965A>G
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ENSP00000472165.2:p.Gly655=
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ENST00000600835.6:c.1965A>G
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ENSP00000470788.1:p.Gly655=
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NM_001290023.1:c.1965A>G
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NP_001276952.1:p.Gly655=
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NM_001290024.1:c.2085A>G
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NP_001276953.1:p.Gly695=
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NM_005535.2:c.1965A>G
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NP_005526.1:p.Gly655=
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XM_006722741.2:c.2085A>G
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XP_006722804.2:p.Gly695=
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XM_011527966.1:c.2118A>G
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XP_011526268.1:p.Gly706=
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|
XM_011527967.1:c.2106A>G
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XP_011526269.1:p.Gly702=
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|
XM_011527968.1:c.2097A>G
|
XP_011526270.1:p.Gly699=
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|
XM_011527969.1:c.2085A>G
|
XP_011526271.1:p.Gly695=
|
|
XM_011527970.1:c.2118A>G
|
XP_011526272.1:p.Gly706=
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|
XM_011527971.1:c.2118A>G
|
XP_011526273.1:p.Gly706=
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|
XM_011527972.1:c.2118A>G
|
XP_011526274.1:p.Gly706=
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|
XM_011527973.1:c.1998A>G
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XP_011526275.1:p.Gly666=
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|
XM_011527974.1:c.1986A>G
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XP_011526276.1:p.Gly662=
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|
XM_011527975.1:c.2085A>G
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XP_011526277.1:p.Gly695=
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|
XM_006722741.3:c.2085A>G
|
XP_006722804.2:p.Gly695=
|
|
XM_011527966.2:c.2118A>G
|
XP_011526268.1:p.Gly706=
|
|
XM_011527967.2:c.2106A>G
|
XP_011526269.1:p.Gly702=
|
|
XM_011527968.3:c.2097A>G
|
XP_011526270.1:p.Gly699=
|
|
XM_011527969.2:c.2085A>G
|
XP_011526271.1:p.Gly695=
|
|
XM_011527970.2:c.2118A>G
|
XP_011526272.1:p.Gly706=
|
|
XM_011527971.3:c.2118A>G
|
XP_011526273.1:p.Gly706=
|
|
XM_011527972.3:c.2118A>G
|
XP_011526274.1:p.Gly706=
|
|
XM_011527973.2:c.1998A>G
|
XP_011526275.1:p.Gly666=
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|
XM_011527974.2:c.1986A>G
|
XP_011526276.1:p.Gly662=
|
|
XM_011527975.2:c.2085A>G
|
XP_011526277.1:p.Gly695=
|
|
XM_017026762.1:c.1383A>G
|
XP_016882251.1:p.Gly461=
|
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NM_001290023.2:c.1965A>G
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NP_001276952.1:p.Gly655=
|
|
NM_005535.3:c.1965A>G
MANE Select
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NP_005526.1:p.Gly655=
|
|