ENST00000703118.1:c.*2835T>G
|
ENSP00000515181.1:n.*2835T>G
|
|
ENST00000703131.1:n.3378T>G
|
|
|
ENST00000703139.1:c.2248T>G
|
|
|
ENST00000703140.1:c.7247T>G
|
ENSP00000515197.1:p.Leu2416Trp
|
|
ENST00000703141.1:c.*2977T>G
|
ENSP00000515198.1:n.*2977T>G
|
|
ENST00000703142.1:c.*4290T>G
|
ENSP00000515199.1:n.*4290T>G
|
|
ENST00000361445.9:c.7460T>G
MANE Select
|
ENSP00000354558.4:p.Leu2487Trp
|
|
ENST00000361445.8:c.7460T>G
|
ENSP00000354558.4:p.Leu2487Trp
|
|
ENST00000376838.5:c.2075T>G
|
ENSP00000366034.1:p.Leu692Trp
|
|
ENST00000455339.1:c.428T>G
|
ENSP00000398745.1:p.Leu143Trp
|
|
ENST00000473471.5:n.472T>G
|
|
|
ENST00000490931.1:n.743T>G
|
|
|
NM_004958.3:c.7460T>G , LRG_734t1:c.7460T>G
|
NP_004949.1:p.Leu2487Trp
|
|
XM_005263438.1:c.7460T>G
|
XP_005263495.1:p.Leu2487Trp
|
|
XM_005263438.2:c.7460T>G
|
XP_005263495.1:p.Leu2487Trp
|
|
XM_017000900.1:c.6779T>G
|
XP_016856389.1:p.Leu2260Trp
|
|
XM_017000901.1:c.6212T>G
|
XP_016856390.1:p.Leu2071Trp
|
|
XM_024446187.1:c.7460T>G
|
XP_024301955.1:p.Leu2487Trp
|
|
XR_001737087.1:n.7498T>G
|
|
|
NM_004958.4:c.7460T>G
MANE Select
|
NP_004949.1:p.Leu2487Trp
|
|
NM_001386500.1:c.7460T>G
|
NP_001373429.1:p.Leu2487Trp
|
|
NM_001386501.1:c.6212T>G
|
NP_001373430.1:p.Leu2071Trp
|
|