ENST00000370096.9:c.2650C>G
MANE Select
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ENSP00000359114.3:p.Pro884Ala
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ENST00000353414.8:c.2533C>G
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ENSP00000302551.6:p.Pro845Ala
|
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ENST00000358392.6:c.2686C>G
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ENSP00000351163.2:p.Pro896Ala
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ENST00000370096.7:c.2650C>G
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ENSP00000359114.3:p.Pro884Ala
|
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ENST00000512756.5:c.2302C>G
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ENSP00000426533.1:p.Pro768Ala
|
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ENST00000635193.1:c.1984C>G
|
|
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NM_001190709.1:c.2533C>G
|
NP_001177638.1:p.Pro845Ala
|
|
NM_001854.3:c.2650C>G
|
NP_001845.3:p.Pro884Ala
|
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NM_080629.2:c.2686C>G
|
NP_542196.2:p.Pro896Ala
|
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NM_080630.3:c.2302C>G
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NP_542197.3:p.Pro768Ala
|
|
XM_011540719.1:c.2650C>G
|
XP_011539021.1:p.Pro884Ala
|
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XM_011540720.1:c.883C>G
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XP_011539022.1:p.Pro295Ala
|
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XM_011540721.1:c.238C>G
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XP_011539023.1:p.Pro80Ala
|
|
XR_946545.1:n.3064C>G
|
|
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NR_134980.1:n.2984C>G
|
|
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XM_017000334.1:c.2803C>G
|
XP_016855823.1:p.Pro935Ala
|
|
XM_017000335.1:c.2797C>G
|
XP_016855824.1:p.Pro933Ala
|
|
XM_017000336.1:c.2803C>G
|
XP_016855825.1:p.Pro935Ala
|
|
XM_017000337.1:c.1201C>G
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XP_016855826.1:p.Pro401Ala
|
|
NM_001854.4:c.2650C>G
MANE Select
|
NP_001845.3:p.Pro884Ala
|
|
NM_080630.4:c.2302C>G
|
NP_542197.3:p.Pro768Ala
|
|
NR_134980.2:n.3010C>G
|
|
|
NM_001190709.2:c.2533C>G
|
NP_001177638.1:p.Pro845Ala
|
|
NM_080629.3:c.2686C>G
|
NP_542196.2:p.Pro896Ala
|
|