ENST00000342741.6:c.696C>G
MANE Select
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ENSP00000339933.4:p.Gly232=
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|
ENST00000342741.4:c.696C>G
|
ENSP00000339933.4:p.Gly232=
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|
ENST00000392414.7:c.603C>G
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ENSP00000376214.3:p.Gly201=
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|
NM_000298.5:c.696C>G
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NP_000289.1:p.Gly232=
|
|
NM_181871.3:c.603C>G
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NP_870986.1:p.Gly201=
|
|
XM_005245266.3:c.855C>G
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XP_005245323.1:p.Gly285=
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XM_006711386.2:c.504C>G
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XP_006711449.1:p.Gly168=
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|
XM_011509639.1:c.855C>G
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XP_011507941.1:p.Gly285=
|
|
XM_011509640.1:c.504C>G
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XP_011507942.1:p.Gly168=
|
|
NM_000298.6:c.696C>G
MANE Select
|
NP_000289.1:p.Gly232=
|
|
XM_006711386.4:c.504C>G
|
XP_006711449.1:p.Gly168=
|
|
XM_011509640.3:c.504C>G
|
XP_011507942.1:p.Gly168=
|
|
XM_017001493.1:c.696C>G
|
XP_016856982.1:p.Gly232=
|
|
NM_181871.4:c.603C>G
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NP_870986.1:p.Gly201=
|
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