ENST00000367698.4:c.902T>A
MANE Select
|
ENSP00000356671.3:p.Val301Glu
|
|
ENST00000367698.3:c.902T>A
|
ENSP00000356671.3:p.Val301Glu
|
|
ENST00000487183.1:n.553T>A
|
|
|
ENST00000617423.4:c.559+2061T>A
|
ENSP00000478688.1:n.559+2061T>A
|
|
NM_000488.3:c.902T>A , LRG_577t1:c.902T>A
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NP_000479.1:p.Val301Glu
|
|
XM_005245198.2:c.758T>A
|
XP_005245255.1:p.Val253Glu
|
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NM_001365052.1:c.758T>A
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NP_001351981.1:p.Val253Glu
|
|
NM_000488.4:c.902T>A
MANE Select
|
NP_000479.1:p.Val301Glu
|
|
NM_001365052.2:c.758T>A
|
NP_001351981.1:p.Val253Glu
|
|
NM_001386302.1:c.1025T>A
|
NP_001373231.1:p.Val342Glu
|
|
NM_001386303.1:c.983T>A
|
NP_001373232.1:p.Val328Glu
|
|
NM_001386304.1:c.881T>A
|
NP_001373233.1:p.Val294Glu
|
|
NM_001386305.1:c.845T>A
|
NP_001373234.1:p.Val282Glu
|
|
NM_001386306.1:c.686T>A
|
NP_001373235.1:p.Val229Glu
|
|