ENST00000336112.9:c.3915A>T
|
ENSP00000337250.5:p.Leu1305=
|
|
ENST00000435504.9:c.3918A>T
MANE Select
|
ENSP00000391447.3:p.Leu1306=
|
|
ENST00000336112.8:c.3834A>T
|
ENSP00000337250.4:p.Leu1278=
|
|
ENST00000404843.5:c.2367A>T
|
ENSP00000383920.1:p.Leu789=
|
|
ENST00000435504.8:c.3918A>T
|
ENSP00000391447.3:p.Leu1306=
|
|
NM_018263.4:c.3918A>T
|
NP_060733.4:p.Leu1306=
|
|
XM_006712039.2:c.3552A>T
|
XP_006712102.1:p.Leu1184=
|
|
XM_006712040.1:c.3138A>T
|
XP_006712103.1:p.Leu1046=
|
|
XM_011532950.1:c.3915A>T
|
XP_011531252.1:p.Leu1305=
|
|
XM_011532951.1:c.3744A>T
|
XP_011531253.1:p.Leu1248=
|
|
NM_018263.5:c.3918A>T
|
NP_060733.4:p.Leu1306=
|
|
XM_006712039.3:c.3552A>T
|
XP_006712102.1:p.Leu1184=
|
|
XM_006712040.2:c.3138A>T
|
XP_006712103.1:p.Leu1046=
|
|
XM_011532950.3:c.3915A>T
|
XP_011531252.1:p.Leu1305=
|
|
XM_011532951.2:c.3744A>T
|
XP_011531253.1:p.Leu1248=
|
|
XM_017004430.1:c.3138A>T
|
XP_016859919.1:p.Leu1046=
|
|
XM_024452974.1:c.4098A>T
|
XP_024308742.1:p.Leu1366=
|
|
NM_001369346.1:c.3744A>T
|
NP_001356275.1:p.Leu1248=
|
|
NM_001369347.1:c.3138A>T
|
NP_001356276.1:p.Leu1046=
|
|
NM_018263.6:c.3918A>T
MANE Select
|
NP_060733.4:p.Leu1306=
|
|