|
ENST00000367698.4:c.820G>C
MANE Select
|
ENSP00000356671.3:p.Ala274Pro
|
|
|
ENST00000367698.3:c.820G>C
|
ENSP00000356671.3:p.Ala274Pro
|
|
|
ENST00000487183.1:n.471G>C
|
|
|
|
ENST00000617423.4:c.559+1979G>C
|
ENSP00000478688.1:n.559+1979G>C
|
|
|
NM_000488.3:c.820G>C , LRG_577t1:c.820G>C
|
NP_000479.1:p.Ala274Pro
|
|
|
XM_005245198.2:c.676G>C
|
XP_005245255.1:p.Ala226Pro
|
|
|
NM_001365052.1:c.676G>C
|
NP_001351981.1:p.Ala226Pro
|
|
|
NM_000488.4:c.820G>C
MANE Select
|
NP_000479.1:p.Ala274Pro
|
|
|
NM_001365052.2:c.676G>C
|
NP_001351981.1:p.Ala226Pro
|
|
|
NM_001386302.1:c.943G>C
|
NP_001373231.1:p.Ala315Pro
|
|
|
NM_001386303.1:c.901G>C
|
NP_001373232.1:p.Ala301Pro
|
|
|
NM_001386304.1:c.799G>C
|
NP_001373233.1:p.Ala267Pro
|
|
|
NM_001386305.1:c.763G>C
|
NP_001373234.1:p.Ala255Pro
|
|
|
NM_001386306.1:c.604G>C
|
NP_001373235.1:p.Ala202Pro
|
|
