ENST00000285071.9:c.775G>T
MANE Select
|
ENSP00000285071.4:p.Ala259Ser
|
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ENST00000285071.8:c.775G>T
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ENSP00000285071.4:p.Ala259Ser
|
|
ENST00000389169.9:c.775G>T
|
ENSP00000373821.5:p.Ala259Ser
|
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ENST00000427497.3:c.149-3451G>T
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ENSP00000394249.3:n.149-3451G>T
|
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ENST00000466317.1:n.618G>T
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|
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ENST00000480316.1:n.741G>T
|
|
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NM_144606.5:c.775G>T
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NP_653207.1:p.Ala259Ser
|
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NM_144997.5:c.775G>T , LRG_325t1:c.775G>T
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NP_659434.2:p.Ala259Ser
|
|
XM_011523714.1:c.829G>T
|
XP_011522016.1:p.Ala277Ser
|
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XM_011523715.1:c.829G>T
|
XP_011522017.1:p.Ala277Ser
|
|
XM_011523716.1:c.829G>T
|
XP_011522018.1:p.Ala277Ser
|
|
XM_011523717.1:c.829G>T
|
XP_011522019.1:p.Ala277Ser
|
|
XM_011523718.1:c.829G>T
|
XP_011522020.1:p.Ala277Ser
|
|
XM_011523719.1:c.829G>T
|
XP_011522021.1:p.Ala277Ser
|
|
XM_011523720.1:c.553G>T
|
XP_011522022.1:p.Ala185Ser
|
|
XM_011523721.1:c.829G>T
|
XP_011522023.1:p.Ala277Ser
|
|
XR_934007.1:n.2169G>T
|
|
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NM_001353229.1:c.829G>T
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NP_001340158.1:p.Ala277Ser
|
|
NM_001353230.1:c.775G>T
|
NP_001340159.1:p.Ala259Ser
|
|
NM_001353231.1:c.775G>T
|
NP_001340160.1:p.Ala259Ser
|
|
NM_144606.6:c.775G>T
|
NP_653207.1:p.Ala259Ser
|
|
NM_144997.6:c.775G>T
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NP_659434.2:p.Ala259Ser
|
|
XM_011523714.3:c.829G>T
|
XP_011522016.1:p.Ala277Ser
|
|
XM_011523718.3:c.829G>T
|
XP_011522020.1:p.Ala277Ser
|
|
XM_011523719.3:c.829G>T
|
XP_011522021.1:p.Ala277Ser
|
|
XM_011523721.3:c.829G>T
|
XP_011522023.1:p.Ala277Ser
|
|
XM_017024305.2:c.829G>T
|
XP_016879794.1:p.Ala277Ser
|
|
XM_017024308.1:c.775G>T
|
XP_016879797.1:p.Ala259Ser
|
|
XM_017024309.2:c.553G>T
|
XP_016879798.1:p.Ala185Ser
|
|
XM_024450635.1:c.829G>T
|
XP_024306403.1:p.Ala277Ser
|
|
XR_001752445.2:n.1333G>T
|
|
|
NM_144997.7:c.775G>T
MANE Select
|
NP_659434.2:p.Ala259Ser
|
|
NM_001353229.2:c.829G>T
|
NP_001340158.1:p.Ala277Ser
|
|
NM_001353230.2:c.775G>T
|
NP_001340159.1:p.Ala259Ser
|
|
NM_001353231.2:c.775G>T
|
NP_001340160.1:p.Ala259Ser
|
|
NM_144606.7:c.775G>T
|
NP_653207.1:p.Ala259Ser
|
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