ENST00000593677.2:c.1672C>G
|
|
|
ENST00000688602.1:c.3069C>G
|
|
|
ENST00000689936.1:c.3041C>G
|
|
|
ENST00000692547.1:n.129C>G
|
|
|
ENST00000359596.8:c.14736C>G
MANE Select
|
ENSP00000352608.2:p.Leu4912=
|
|
ENST00000355481.8:c.14721C>G
|
ENSP00000347667.3:p.Leu4907=
|
|
ENST00000359596.7:c.14736C>G
|
ENSP00000352608.2:p.Leu4912=
|
|
ENST00000360985.7:c.14718C>G
|
ENSP00000354254.4:p.Leu4906=
|
|
NM_000540.2:c.14736C>G , LRG_766t1:c.14736C>G
|
NP_000531.2:p.Leu4912=
|
|
NM_001042723.1:c.14721C>G
|
NP_001036188.1:p.Leu4907=
|
|
XM_006723317.1:c.14718C>G
|
XP_006723380.1:p.Leu4906=
|
|
XM_006723319.1:c.14703C>G
|
XP_006723382.1:p.Leu4901=
|
|
XM_011527204.1:c.14733C>G
|
XP_011525506.1:p.Leu4911=
|
|
XM_011527205.1:c.14649C>G
|
XP_011525507.1:p.Leu4883=
|
|
XM_006723317.2:c.14718C>G
|
XP_006723380.1:p.Leu4906=
|
|
XM_006723319.2:c.14703C>G
|
XP_006723382.1:p.Leu4901=
|
|
XM_011527205.2:c.14649C>G
|
XP_011525507.1:p.Leu4883=
|
|
NM_000540.3:c.14736C>G
MANE Select
|
NP_000531.2:p.Leu4912=
|
|
NM_001042723.2:c.14721C>G
|
NP_001036188.1:p.Leu4907=
|
|