ENST00000225964.10:c.4188C>G
MANE Select
|
ENSP00000225964.6:p.Ile1396Met
|
|
ENST00000225964.9:c.4188C>G
|
ENSP00000225964.5:p.Ile1396Met
|
|
NM_000088.3:c.4188C>G , LRG_1t1:c.4188C>G
|
NP_000079.2:p.Ile1396Met
|
|
XM_005257058.3:c.3918C>G
|
XP_005257115.2:p.Ile1306Met
|
|
XM_005257059.3:c.3270C>G
|
XP_005257116.2:p.Ile1090Met
|
|
XM_011524341.1:c.3990C>G
|
XP_011522643.1:p.Ile1330Met
|
|
XM_005257058.4:c.3918C>G
|
XP_005257115.2:p.Ile1306Met
|
|
XM_005257059.4:c.3270C>G
|
XP_005257116.2:p.Ile1090Met
|
|
NM_000088.4:c.4188C>G
MANE Select
|
NP_000079.2:p.Ile1396Met
|
|