ENST00000302450.11:c.694G>T
MANE Select
|
ENSP00000305204.6:p.Val232Phe
|
|
ENST00000302450.10:c.694G>T
|
ENSP00000305204.6:p.Val232Phe
|
|
ENST00000435431.5:c.478+216G>T
|
ENSP00000414834.1:n.478+216G>T
|
|
NM_001304361.1:c.199G>T
|
NP_001291290.1:p.Val67Phe
|
|
NM_152515.4:c.694G>T
|
NP_689728.3:p.Val232Phe
|
|
NR_130712.1:n.557+216G>T
|
|
|
XM_011510666.1:c.199G>T
|
XP_011508968.1:p.Val67Phe
|
|
XM_011510666.2:c.199G>T
|
XP_011508968.1:p.Val67Phe
|
|
NM_152515.5:c.694G>T
MANE Select
|
NP_689728.3:p.Val232Phe
|
|
NM_001304361.2:c.199G>T
|
NP_001291290.1:p.Val67Phe
|
|
NR_130712.2:n.489+216G>T
|
|
|