ENST00000359678.10:c.1139G=
MANE Select
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ENSP00000352706.5:p.Gly380=
|
|
ENST00000359678.9:c.1139G=
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ENSP00000352706.5:p.Gly380=
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|
ENST00000392332.7:c.*88G=
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ENSP00000376144.3:n.*88G=
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|
ENST00000399855.2:c.94G=
|
|
|
ENST00000410045.5:c.470G=
|
ENSP00000386274.1:p.Gly157=
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|
ENST00000486981.1:n.374G=
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|
|
ENST00000622246.4:c.1121G=
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ENSP00000481055.1:p.Gly374=
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|
NM_014362.3:c.1139G=
|
NP_055177.2:p.Gly380=
|
|
NM_198047.2:c.*88G=
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NP_932164.1:n.*88G=
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|
XM_011510953.1:c.1139G=
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XP_011509255.1:p.Gly380=
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|
XM_011510954.1:c.641G=
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XP_011509256.1:p.Gly214=
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|
XR_922903.1:n.1349G=
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|
|
XM_011510953.2:c.1139G=
|
XP_011509255.1:p.Gly380=
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|
XR_922903.2:n.1168G=
|
|
|
NM_014362.4:c.1139G=
MANE Select
|
NP_055177.2:p.Gly380=
|
|
NM_198047.3:c.*88G=
|
NP_932164.1:n.*88G=
|
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