ENST00000313468.10:c.484G>T
MANE Select
|
ENSP00000315774.5:p.Val162Leu
|
|
ENST00000313468.9:c.484G>T
|
ENSP00000315774.5:p.Val162Leu
|
|
ENST00000524810.5:c.416G>T
|
|
|
ENST00000526339.5:c.484G>T
|
ENSP00000436287.1:p.Val162Leu
|
|
ENST00000526446.5:c.*539G>T
|
ENSP00000433645.1:n.*539G>T
|
|
ENST00000528492.1:c.46G>T
|
ENSP00000432848.1:p.Val16Leu
|
|
ENST00000531282.1:n.336G>T
|
|
|
NM_002496.3:c.484G>T
|
NP_002487.1:p.Val162Leu
|
|
XM_005274013.1:c.484G>T
|
XP_005274070.1:p.Val162Leu
|
|
XM_005274014.1:c.484G>T
|
XP_005274071.1:p.Val162Leu
|
|
XM_005274015.1:c.364G>T
|
XP_005274072.1:p.Val122Leu
|
|
XM_011545053.1:c.484G>T
|
XP_011543355.1:p.Val162Leu
|
|
NM_002496.4:c.484G>T
MANE Select
|
NP_002487.1:p.Val162Leu
|
|