|
ENST00000367698.4:c.902T>C
MANE Select
|
ENSP00000356671.3:p.Val301Ala
|
|
|
ENST00000367698.3:c.902T>C
|
ENSP00000356671.3:p.Val301Ala
|
|
|
ENST00000487183.1:n.553T>C
|
|
|
|
ENST00000617423.4:c.559+2061T>C
|
ENSP00000478688.1:n.559+2061T>C
|
|
|
NM_000488.3:c.902T>C , LRG_577t1:c.902T>C
|
NP_000479.1:p.Val301Ala
|
|
|
XM_005245198.2:c.758T>C
|
XP_005245255.1:p.Val253Ala
|
|
|
NM_001365052.1:c.758T>C
|
NP_001351981.1:p.Val253Ala
|
|
|
NM_000488.4:c.902T>C
MANE Select
|
NP_000479.1:p.Val301Ala
|
|
|
NM_001365052.2:c.758T>C
|
NP_001351981.1:p.Val253Ala
|
|
|
NM_001386302.1:c.1025T>C
|
NP_001373231.1:p.Val342Ala
|
|
|
NM_001386303.1:c.983T>C
|
NP_001373232.1:p.Val328Ala
|
|
|
NM_001386304.1:c.881T>C
|
NP_001373233.1:p.Val294Ala
|
|
|
NM_001386305.1:c.845T>C
|
NP_001373234.1:p.Val282Ala
|
|
|
NM_001386306.1:c.686T>C
|
NP_001373235.1:p.Val229Ala
|
|
