|
ENST00000367698.4:c.929A>C
MANE Select
|
ENSP00000356671.3:p.Asp310Ala
|
|
|
ENST00000367698.3:c.929A>C
|
ENSP00000356671.3:p.Asp310Ala
|
|
|
ENST00000487183.1:n.580A>C
|
|
|
|
ENST00000617423.4:c.559+2088A>C
|
ENSP00000478688.1:n.559+2088A>C
|
|
|
NM_000488.3:c.929A>C , LRG_577t1:c.929A>C
|
NP_000479.1:p.Asp310Ala
|
|
|
XM_005245198.2:c.785A>C
|
XP_005245255.1:p.Asp262Ala
|
|
|
NM_001365052.1:c.785A>C
|
NP_001351981.1:p.Asp262Ala
|
|
|
NM_000488.4:c.929A>C
MANE Select
|
NP_000479.1:p.Asp310Ala
|
|
|
NM_001365052.2:c.785A>C
|
NP_001351981.1:p.Asp262Ala
|
|
|
NM_001386302.1:c.1052A>C
|
NP_001373231.1:p.Asp351Ala
|
|
|
NM_001386303.1:c.1010A>C
|
NP_001373232.1:p.Asp337Ala
|
|
|
NM_001386304.1:c.908A>C
|
NP_001373233.1:p.Asp303Ala
|
|
|
NM_001386305.1:c.872A>C
|
NP_001373234.1:p.Asp291Ala
|
|
|
NM_001386306.1:c.713A>C
|
NP_001373235.1:p.Asp238Ala
|
|
