|
ENST00000367698.4:c.789T>A
MANE Select
|
ENSP00000356671.3:p.Pro263=
|
|
|
ENST00000367698.3:c.789T>A
|
ENSP00000356671.3:p.Pro263=
|
|
|
ENST00000487183.1:n.440T>A
|
|
|
|
ENST00000617423.4:c.559+1948T>A
|
ENSP00000478688.1:n.559+1948T>A
|
|
|
NM_000488.3:c.789T>A , LRG_577t1:c.789T>A
|
NP_000479.1:p.Pro263=
|
|
|
XM_005245198.2:c.645T>A
|
XP_005245255.1:p.Pro215=
|
|
|
NM_001365052.1:c.645T>A
|
NP_001351981.1:p.Pro215=
|
|
|
NM_000488.4:c.789T>A
MANE Select
|
NP_000479.1:p.Pro263=
|
|
|
NM_001365052.2:c.645T>A
|
NP_001351981.1:p.Pro215=
|
|
|
NM_001386302.1:c.912T>A
|
NP_001373231.1:p.Pro304=
|
|
|
NM_001386303.1:c.870T>A
|
NP_001373232.1:p.Pro290=
|
|
|
NM_001386304.1:c.768T>A
|
NP_001373233.1:p.Pro256=
|
|
|
NM_001386305.1:c.763-31T>A
|
NP_001373234.1:n.763-31T>A
|
|
|
NM_001386306.1:c.573T>A
|
NP_001373235.1:p.Pro191=
|
|
