ENST00000367698.4:c.848T>C
MANE Select
|
ENSP00000356671.3:p.Met283Thr
|
|
ENST00000367698.3:c.848T>C
|
ENSP00000356671.3:p.Met283Thr
|
|
ENST00000487183.1:n.499T>C
|
|
|
ENST00000617423.4:c.559+2007T>C
|
ENSP00000478688.1:n.559+2007T>C
|
|
NM_000488.3:c.848T>C , LRG_577t1:c.848T>C
|
NP_000479.1:p.Met283Thr
|
|
XM_005245198.2:c.704T>C
|
XP_005245255.1:p.Met235Thr
|
|
NM_001365052.1:c.704T>C
|
NP_001351981.1:p.Met235Thr
|
|
NM_000488.4:c.848T>C
MANE Select
|
NP_000479.1:p.Met283Thr
|
|
NM_001365052.2:c.704T>C
|
NP_001351981.1:p.Met235Thr
|
|
NM_001386302.1:c.971T>C
|
NP_001373231.1:p.Met324Thr
|
|
NM_001386303.1:c.929T>C
|
NP_001373232.1:p.Met310Thr
|
|
NM_001386304.1:c.827T>C
|
NP_001373233.1:p.Met276Thr
|
|
NM_001386305.1:c.791T>C
|
NP_001373234.1:p.Met264Thr
|
|
NM_001386306.1:c.632T>C
|
NP_001373235.1:p.Met211Thr
|
|