ENST00000367698.4:c.940G>T
MANE Select
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ENSP00000356671.3:p.Val314Phe
|
|
ENST00000367698.3:c.940G>T
|
ENSP00000356671.3:p.Val314Phe
|
|
ENST00000487183.1:n.591G>T
|
|
|
ENST00000617423.4:c.559+2099G>T
|
ENSP00000478688.1:n.559+2099G>T
|
|
NM_000488.3:c.940G>T , LRG_577t1:c.940G>T
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NP_000479.1:p.Val314Phe
|
|
XM_005245198.2:c.796G>T
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XP_005245255.1:p.Val266Phe
|
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NM_001365052.1:c.796G>T
|
NP_001351981.1:p.Val266Phe
|
|
NM_000488.4:c.940G>T
MANE Select
|
NP_000479.1:p.Val314Phe
|
|
NM_001365052.2:c.796G>T
|
NP_001351981.1:p.Val266Phe
|
|
NM_001386302.1:c.1063G>T
|
NP_001373231.1:p.Val355Phe
|
|
NM_001386303.1:c.1021G>T
|
NP_001373232.1:p.Val341Phe
|
|
NM_001386304.1:c.919G>T
|
NP_001373233.1:p.Val307Phe
|
|
NM_001386305.1:c.883G>T
|
NP_001373234.1:p.Val295Phe
|
|
NM_001386306.1:c.724G>T
|
NP_001373235.1:p.Val242Phe
|
|