ENST00000649046.1:c.12259G>T
MANE Select
|
ENSP00000496870.1:p.Val4087Phe
|
|
ENST00000649153.1:c.3159G>T
|
|
|
ENST00000650252.1:c.1287G>T
|
ENSP00000496887.1:p.Leu429=
|
|
ENST00000263816.7:c.12259G>T
|
ENSP00000263816.3:p.Val4087Phe
|
|
NM_004525.2:c.12259G>T
|
NP_004516.2:p.Val4087Phe
|
|
XM_011511183.1:c.12130G>T
|
XP_011509485.1:p.Val4044Phe
|
|
XM_011511184.1:c.9970G>T
|
XP_011509486.1:p.Val3324Phe
|
|
NM_004525.3:c.12259G>T
MANE Select
|
NP_004516.2:p.Val4087Phe
|
|
XM_011511183.3:c.12130G>T
|
XP_011509485.1:p.Val4044Phe
|
|
XM_011511184.2:c.9970G>T
|
XP_011509486.1:p.Val3324Phe
|
|