ENST00000367698.4:c.1388T>C
MANE Select
|
ENSP00000356671.3:p.Val463Ala
|
|
ENST00000367698.3:c.1388T>C
|
ENSP00000356671.3:p.Val463Ala
|
|
ENST00000617423.4:c.773T>C
|
ENSP00000478688.1:p.Val258Ala
|
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NM_000488.3:c.1388T>C , LRG_577t1:c.1388T>C
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NP_000479.1:p.Val463Ala
|
|
XM_005245198.2:c.1244T>C
|
XP_005245255.1:p.Val415Ala
|
|
NM_001365052.1:c.1244T>C
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NP_001351981.1:p.Val415Ala
|
|
NM_000488.4:c.1388T>C
MANE Select
|
NP_000479.1:p.Val463Ala
|
|
NM_001365052.2:c.1244T>C
|
NP_001351981.1:p.Val415Ala
|
|
NM_001386302.1:c.1511T>C
|
NP_001373231.1:p.Val504Ala
|
|
NM_001386303.1:c.1469T>C
|
NP_001373232.1:p.Val490Ala
|
|
NM_001386304.1:c.1367T>C
|
NP_001373233.1:p.Val456Ala
|
|
NM_001386305.1:c.1331T>C
|
NP_001373234.1:p.Val444Ala
|
|
NM_001386306.1:c.1172T>C
|
NP_001373235.1:p.Val391Ala
|
|