ENST00000367698.4:c.1240G>C
MANE Select
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ENSP00000356671.3:p.Ala414Pro
|
|
ENST00000367698.3:c.1240G>C
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ENSP00000356671.3:p.Ala414Pro
|
|
ENST00000617423.4:c.625G>C
|
ENSP00000478688.1:p.Ala209Pro
|
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NM_000488.3:c.1240G>C , LRG_577t1:c.1240G>C
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NP_000479.1:p.Ala414Pro
|
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XM_005245198.2:c.1096G>C
|
XP_005245255.1:p.Ala366Pro
|
|
NM_001365052.1:c.1096G>C
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NP_001351981.1:p.Ala366Pro
|
|
NM_000488.4:c.1240G>C
MANE Select
|
NP_000479.1:p.Ala414Pro
|
|
NM_001365052.2:c.1096G>C
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NP_001351981.1:p.Ala366Pro
|
|
NM_001386302.1:c.1363G>C
|
NP_001373231.1:p.Ala455Pro
|
|
NM_001386303.1:c.1321G>C
|
NP_001373232.1:p.Ala441Pro
|
|
NM_001386304.1:c.1219G>C
|
NP_001373233.1:p.Ala407Pro
|
|
NM_001386305.1:c.1183G>C
|
NP_001373234.1:p.Ala395Pro
|
|
NM_001386306.1:c.1024G>C
|
NP_001373235.1:p.Ala342Pro
|
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