ENST00000225964.10:c.4381G>T
MANE Select
|
ENSP00000225964.6:p.Val1461Phe
|
|
ENST00000225964.9:c.4381G>T
|
ENSP00000225964.5:p.Val1461Phe
|
|
NM_000088.3:c.4381G>T , LRG_1t1:c.4381G>T
|
NP_000079.2:p.Val1461Phe
|
|
XM_005257058.3:c.4111G>T
|
XP_005257115.2:p.Val1371Phe
|
|
XM_005257059.3:c.3463G>T
|
XP_005257116.2:p.Val1155Phe
|
|
XM_011524341.1:c.4183G>T
|
XP_011522643.1:p.Val1395Phe
|
|
XM_005257058.4:c.4111G>T
|
XP_005257115.2:p.Val1371Phe
|
|
XM_005257059.4:c.3463G>T
|
XP_005257116.2:p.Val1155Phe
|
|
NM_000088.4:c.4381G>T
MANE Select
|
NP_000079.2:p.Val1461Phe
|
|