ENST00000355697.7:c.733-1G>C
MANE Select
|
ENSP00000347924.2:n.733-1G>C
|
|
ENST00000355697.6:c.733-1G>C
|
ENSP00000347924.2:n.733-1G>C
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|
ENST00000369131.8:c.385-1G>C
|
ENSP00000358127.4:n.385-1G>C
|
|
ENST00000461438.5:n.762-1G>C
|
|
|
ENST00000466218.5:n.682-1G>C
|
|
|
ENST00000484960.5:n.63-1G>C
|
|
|
ENST00000490417.6:n.196-1G>C
|
|
|
NM_213649.1:c.733-1G>C
|
NP_998814.1:n.733-1G>C
|
|
NR_110305.1:n.751-1G>C
|
|
|
XM_005269525.3:c.706-1G>C
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XP_005269582.1:n.706-1G>C
|
|
XM_005269526.1:c.385-1G>C
|
XP_005269583.1:n.385-1G>C
|
|
XM_005269527.1:c.385-1G>C
|
XP_005269584.1:n.385-1G>C
|
|
XM_011539282.1:c.385-1G>C
|
XP_011537584.1:n.385-1G>C
|
|
XR_945603.1:n.795-1G>C
|
|
|
XM_005269525.5:c.706-1G>C
|
XP_005269582.1:n.706-1G>C
|
|
XM_005269526.2:c.385-1G>C
|
XP_005269583.1:n.385-1G>C
|
|
XM_011539282.2:c.385-1G>C
|
XP_011537584.1:n.385-1G>C
|
|
XM_024447793.1:c.385-1G>C
|
XP_024303561.1:n.385-1G>C
|
|
XR_001747022.1:n.984-1G>C
|
|
|
XR_001747023.1:n.878-1G>C
|
|
|
XR_945603.3:n.814-1G>C
|
|
|
NM_213649.2:c.733-1G>C
MANE Select
|
NP_998814.1:n.733-1G>C
|
|