ENST00000367698.4:c.1306G>C
MANE Select
|
ENSP00000356671.3:p.Ala436Pro
|
|
ENST00000367698.3:c.1306G>C
|
ENSP00000356671.3:p.Ala436Pro
|
|
ENST00000617423.4:c.691G>C
|
ENSP00000478688.1:p.Ala231Pro
|
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NM_000488.3:c.1306G>C , LRG_577t1:c.1306G>C
|
NP_000479.1:p.Ala436Pro
|
|
XM_005245198.2:c.1162G>C
|
XP_005245255.1:p.Ala388Pro
|
|
NM_001365052.1:c.1162G>C
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NP_001351981.1:p.Ala388Pro
|
|
NM_000488.4:c.1306G>C
MANE Select
|
NP_000479.1:p.Ala436Pro
|
|
NM_001365052.2:c.1162G>C
|
NP_001351981.1:p.Ala388Pro
|
|
NM_001386302.1:c.1429G>C
|
NP_001373231.1:p.Ala477Pro
|
|
NM_001386303.1:c.1387G>C
|
NP_001373232.1:p.Ala463Pro
|
|
NM_001386304.1:c.1285G>C
|
NP_001373233.1:p.Ala429Pro
|
|
NM_001386305.1:c.1249G>C
|
NP_001373234.1:p.Ala417Pro
|
|
NM_001386306.1:c.1090G>C
|
NP_001373235.1:p.Ala364Pro
|
|