ENST00000216927.4:c.753G=
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ENSP00000216927.4:p.Pro251=
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|
ENST00000303415.7:c.1086G=
MANE Select
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ENSP00000305529.3:p.Pro362=
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|
ENST00000344103.8:c.435G=
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ENSP00000342759.4:p.Pro145=
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ENST00000381580.5:c.987G=
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ENSP00000370992.1:p.Pro329=
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ENST00000381583.6:c.753G=
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ENSP00000370995.2:p.Pro251=
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|
ENST00000478145.6:n.147G=
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|
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ENST00000497407.2:n.235G=
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|
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NM_001039508.1:c.753G=
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NP_001034597.1:p.Pro251=
|
|
NM_018556.3:c.1086G=
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NP_061026.2:p.Pro362=
|
|
NM_080816.2:c.435G=
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NP_543006.2:p.Pro145=
|
|
XM_005260749.2:c.768G=
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XP_005260806.1:p.Pro256=
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|
XM_011529286.1:c.987G=
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XP_011527588.1:p.Pro329=
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|
XM_005260749.4:c.768G=
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XP_005260806.1:p.Pro256=
|
|
XM_011529286.2:c.987G=
|
XP_011527588.1:p.Pro329=
|
|
NM_018556.4:c.1086G=
MANE Select
|
NP_061026.2:p.Pro362=
|
|
NM_080816.3:c.435G=
|
NP_543006.2:p.Pro145=
|
|
NM_001039508.2:c.753G=
|
NP_001034597.1:p.Pro251=
|
|